What is described in your message seems to have been my experience now for over 5 years. Would an NMDA blocker help with this - one like Namenda/Axura or dextromethorphan? I have not been diagnosed with Alzheimers, but have chemical sensitivities where the reactions include some of the same symptoms as some neurological problems. If I can just stay away from the chemical fumes, I mostly do okay, but if I get into the fumes it is bad news. I heard about the Axura being used in Germany for ten years or so and that the FDA has recently approved the same thing in the USA but under the name Namenda - it is all memantine(sp?) I think this medicine is supposed to protect brain/nerve cells from dying. Anyway, there is a study by Dr. Martin Pall on NMDA blockers and MCS in the Townsend Letter withing the last couple of months, and that might me a place to start looking. I would appreciate any other information, help, comments, as I am considering trying the Namenda. I could not use the dextrmethorphan due to its CYP2D6 clearance. I have been doing alternative therapies, and I am doing good when not exposed to the fumes, it is just that those really bad reactions still happen upon exposures.

QUINOLINE (Benzopyridine), C9H7N, an organic base first obtained from coal-tar in 1834 by F. Runge (Pogg. Ann., 1834, 31, p. 68), and later by C. Gerhardt by the distillation of cinchonine, quinine and other alkaloids with caustic potash (Ann., 1842, 42, p. 310; 44, p. 279). It also occurs with pynidine and its homologues in bone-oil. It may be prepared by distilling cinchoninic acid with lime; by the reduction of ortho-aminocinnamic aldehyde (A. Baeyer and V. Drewson, Ber., 1883, 16, p. 2207); by passing the vapour of allyl aniline over heated lead oxide; by the condensation of ortho-aminobenzaidehyde with acetaldehyde in. the presence of aqueous caustic soda (P. Friedlnder and C. F. Gohring, Ber., 1882, 15, p. 2572; 1883, 16, p. 1833); by the action of orthotoluidine on glyoxal at 550 C. (V. Kulisch, Monats., 1894, 15, p. 276); by the action of phosphorus pentachloride on hydrocarbostyril (the inner anhydride of ortho-aminohydrocinnamic acid), the chlorinated compound first formed being then reduced by hydriodic acid (A. Baeyer):

,CH2-CH2 ,CH=C.Cl /CHCH

C6H4 ~ CsH~ ~C6H4 I

~NH - CO N = C.Cl N = CH

and by the so-called Skraup reaction, which consists in oxidizing a mixture of aniline, glycerin and concentrated sulphuric acid, with nitrobenzene (Z. Skraup, Monats., 1880, I, p. 316; 1881, 2, p. 141). This reaction is a very violent one, and its mechanism may probably be explained as follows: The glycerin is first converted into acrolein, which combines with the aniline to form acrolein-aniline, and this product is then oxidized by the nitrobenzene:

C3H5O3*CIHsO ( C6H5NH2) ~C6H5N: CH CH: CH2*C,H7N.

The nitrobenzene may be replaced by arsenic acid, when the reaction proceeds much more quietly and a cleaner product is obtained (C. A. Knueppel, Ber., 1896, 29, p. 703). The Skraup reaction is a perfectly general one for primary amino-compounds; the halogen-, nitro- and oxy-anilines (aminophenols) react similarly, as do also the toluidines, naphthylamines, aminoanthracene, meta- and para-phenylene diamines, and orthoand ~y-aminoquinoline.

Quinoline is a colorless liquid with a smell resembling that of pyridine. It boils at 238 C. and is very hygroscopic. It is a tertiary base and forms well-defined salts. It is almost insoluble in water, but dissolves readily in the common organic solvents. It combines readily with the alkyl halides. H. Decker (Ber., 1905, 38, p. 1144) has found that many ortho substituted quinolines will not combine with methyl Iodide owing to steric hindrance, but the difficulty can be overcome in most cases by using methyl sulphate and heating the reaction components to 100 C. for half an hour. Nitric acid and chromic acid have little action on quinoline, but alkaline potassium permanganate oxidizes it to carbon dioxide, ammonia, oxalic, and quinolinic acids (S. Hoogewerif and W. A. v. Dorp, Rec. Pays Bas, 1882, I, p. 107). Bleaching powder oxidizes it to chlorcarbostyril.

a j It is reduced by the action of zinc and ammonia p to di-and tetra-hydroquinolines. A hexahydro and a decahydroquinoline have been obtained N a by heating tetrahydroquinoline with hydri o odic acid and phosphorus to high temperatures (E. Bamberger, Ber., 1890, 23, p. 1138). Numerous substitution products of quinoline are known, and the positions in the molecule are generally designated in accordance with the scheme shown in the inset formula: the letters o, in, p, a, standing for ort/zo-, ineta-, para-, and ana-.

The oxvquinolines possess a certain importance owing to their relationship to the alkaloids. Those with the hydroxyl group in the benzene nucleus are prepared from the aminophenols by the Skraup reaction. Only two are known containing the hydroxyl group in the pyridine nucleus, namely, carbostyril (a-oxyquinoline), which is formed by the reduction of ortho-aminocinnamic acid with ammonium suiphide (L. Chiozza, Ann., 1852, 83, p. 118) or with ferrous sulphate and baryta, and kynurine (y-oxyquinoline), which is obtained by the action of nitrous acid on y-aminoquinoline (A. Claus and H. Howitz, Jour. prak. C/fern., 1894, 158, p. 232). It is also formed by the condensation of anthranilic acid with acetaldehyde (S. Niemeritowski, Ber., 1895, 28, p. 2811). They are both crystalline solids, the former melting when anhydrous at f99200, and the latter at 52 C.

Of the homologues of quinoline, the most important are quinaldine, lepidine, -y-phenylquinoline, and flavoline. Quinaldine (a-methvlquinoline) is present in coal-tar; it may be prepared by condensing aniline with paraldehyde and concentrated hydrochloric acid (0. Doebner and W. v. Miller, Ber., 1881, 14, pp. 2812 et seq.). The reaction is a perfectly general one, for the aniline may be replaced by other aromatic amines and the aldehyde by other aldehydes, and so a large number of quinoline homologues may be prepared in this way. Quinaldine may also be obtained by condensing ortho-aminobenzaldehyde with acetone in presence of caustic soda (P. Friedlander, bc. cit.). It is a colorless liquid which boils at 247 C. The Cl-I, group is very reactive, condensing readily with aldehydes and with phthalic anhydride. Potassium permanganate oxidizes it to acetylanthranilic acid, HOOC(l)-C,H4.(2)NH.COCH,, while chromic acid oxidizes it to quinaldic acid (quinoline-a-carboxylic acid). Lepidine(y-methylqurnoline) was first obtained by distilling cinchonine with caustic potash. It may be prepared synthetically by condensing ortho-aminoacetophenone with paraldehyde and caustic soda (L. Knorr, Ann., 1886, 236, p. 69) or from aniline, acetone, formaldehyde and hydrochloric acid (C. Beyer, Jour. prak. Chem., 1885, 140, p. 125). It may also be prepared by condensing cv.y-dimethylquinoline and formaldehyde, the resulting a-ethanollepidine, C,H5.CH,N(CH2.CH1.OH), breaks clown on. heating and forms lepidine (W. Konigs and ,A. Mengel, Ber., 1904, 37, p. 1322). It is a colorless liquid which boils at 255 C. Chromic acid oxidizes it to cinchoninic acid (see below), whilst potassium permanganate oxidizes it to lepidinic acid (-y-methylquinolinic acid) and cinchomeronic acid (see PYRIDINE). -y-Phenylguinoline, which is probably the parent substance of the cinchona alkaloids, is prepared by heating ~-phetiylquinvldic acid, the oxidation product of the -y-phenylquinaldine, which results from the action of alcoholic potash on a mixture of orthoaminobenzophenone and acetone (W. KOnigs and R. Geigy, ]3er., 1885, 18, p. 2400), or by the action of sulphuric acid on Lenzoylacetone anilide (C. Beyer, Ber., 1887, 20, p. 1767). It crystallizes in needles which melt at 61 C. F/ave/me (a-phenyl-y-methylquinoline) is formed on heating flavenol (see below) with excess of zinc dust, or by heating molecular proportions of ortho-aminoacetophenone and acetophenone, in dilute alcoholic solution, with a sniall quantity of 10% caustic soda solution (0. Fischer, Ber., I886, 19, p. 1037). Closely related to flavoline is flavaniline or (a)-para-aminophenyl-~-methylquinoline, which is formed when acetanilide and anhydrous zinc chloride are heated together for many hours at 250270 C. (0. Fischer and C. Rudolph, Ber., 1682, 15, p. 1500), or by heating ortho- and para-aminoacetophenone with zinc chloride to 90 C. (0. Fischer, Ber., 1886, i9, p. 1038). It crystallizes from benzene in prismsr which melt at 97 C. Sodium nitrite in the presence of excess uf acid converts it into the corresponding hydroxylic compound .fiavenol.

The oxy derivatives of the quinoline homologues are best obtained from the aniline derivatives of j3-ketonic acids. At 110 C. aniline and acetoacetic ester condense to form anilido-acetoacetic ester, CHiCO. CH,. CO~ NH .C6H5, which is converted by concentrated acids into a-oxy-y-methylquinoline (L. Knorr, Ann., 1886,236, p. 73). On the other hand, at about 240 C., the amine and ester react to form $-anilidocrotonic ester, CH3.C(NHC6H5) : CH~COOC2Fl5, which yields y-oxy-a-methylquinoline (M. Conrad and L. Limpach, Ber., 1887, 20, p. 947).

Numerous carboxylic acids of quinoline are known, - the most important of which are quinaldic, cinchoninic and acridinic acids. Quinaldic acid (quinoline-a-carboxylic acid) is produced when quinaldine is oxidized by chromic acid. It crystallizes in needles, which contain two molecules of water of crystallization, and melt at I56 C. When heated above the melting-point it loses carbon dioxide and yields quinoline. Alkaline potassium pernanganate oxidizes it to pyridine tricarboxylic acid (2.3.6). Cinchoninic acid (quinoline-y-carboxylic acid) is formed when cinchonine is oxidized by nitric acid, or by the oxidation of lepidine. It crystallizes from water in needles or prisms and in the anhydrous state melts at 253254 C. Potassium permanganate oxidizes it to pyridine tricarboxylic acid (2.3.4). A cridinic acid (quinoline-a$dicarboxylic acid) is formed when acridine is oxidized by potassium permanganate (C. Graebe and H. Caro, Ber., 1880, 13, p. lao). It crystallizes in needles, which are easily soluble in alcohol, and when heated above 130 C. lose carbon dioxide and leave a residue of quinoline-i3-carboxylic acid.

Isoquinoline, isomeric with quinoline, was first discovered in coal-tar in 1885 by S. Hoogewerif and W. A. v. Dorp (Rec. Pays Bas, I 885, 4, 125); its formula is shown in the inset. It may be separated from the quinoline which accompanies it by means of the difference in the solubility of the sulphates of the two compounds, N

isoquinoline sulphate being much less soluble than -

quinoline sulphate. It may be prepared by passing Isoquinohne.

the vapour of benzylidene ethylamine through a red-hot tube (A. Pictet and S. Popovici, Ber., 1892, 25, p. 733); by the action of concentrated sulphuric acid on benzyl amino-acetaldehyde, C~H5CH1NH~CH2~CHO (E. Fischer), or on benzylidene aminoacetal, C6H5CH : N . CH~ . CH(OC2H6)i (C. Pomeranz, Monats., 1892, 14, p. 116); by heating cinnamenyl aldoxime with phosphorus pentoxide to 70 C. (E. Bamberger, Ber., 1894, 27, p. 1955), CEHSCH : CH.CH : NOH. s~C6H5CH : CHNH.COH]sC,H7N;

by the action of hydriodic acid on the oxydichiorisoquinoline formed when phosphorus pentachloride reacts with hippuric acid; by the distillation of homophthalimide over zinc dust (M. Le Blanc, Ber., 1888, 21, p. 2299), or by treatment with phosphorus oxychloride followed by the reduction of the resulting dichlorisoquinoline with hydriodic acid (S. Gabriel, Ber., 1886, 19, pp. 1655, 2355):

/cH2co /dH C(OH) /cH= c-cl /cH~-cH

I or C6Hu~ I -~ C6H~< I s c6ii4~

\C0NH \C(0Hl: N \c-C1=N \cH=

It is also formed from isubenzalphthalide by the action of ammonia, followed by phosphorus oxychloride and reduction of the chlorinated product (S. Gabriel),

/cH= c-ciIl, /cH= C-C,H,

c,He~ I ~c6n4< I

\C0-O \CONH

/cH=cc,H~ /cH~~ c-c,H,

.~ci114< I sc,H4K I

\ccl=N \CH=N

and from isocoumarin carboxylic acid by conversion into isocarbostyril on heating, and subsequent reduction by distillation with zinc dust (E. Bamberger, Ber., 1892, 25, p. 1138). It melts at 2223 C. and boils at 240 C., and behaves in most respects similarly to quinoline. By oxidation with alkaline potassium permanganate it yields phthalic acid and cinchomeronic acid. Reduction by means of tin and hydrochloric acid gives a tetrahydro derivative.

Numerous derivatives of isoquinoline are obtained in the decomposition of various vegetable alkaloids. Papaverine on fusion

one, and its mechanism may probably be explained as follows: The glycerin is first converted into acrolein, which combines with the aniline to form acrolein-aniline, and this product is then oxidized by the nitrobenzene:

C3H5O3*CIHsO ( C6H5NH2) ~C6H5N: CH CH: CH2*C,H7N.

The nitrobenzene may be replaced by arsenic acid, when the reaction proceeds much more quietly and a cleaner product is obtained (C. A. Knueppel, Ber., 1896, 29, p. 703). The Skraup reaction is a perfectly general one for primary amino-compounds; the halogen-, nitro- and oxy-anilines (aminophenols) react similarly, as do also the toluidines, naphthylamines, aminoanthracene, meta- and para-phenylene diamines, and orthoand ~y-aminoquinoline.

Quinoline is a colorless liquid with a smell resembling that of pyridine. It boils at 238 C. and is very hygroscopic. It is a tertiary base and forms well-defined salts. It is almost insoluble in water, but dissolves readily in the common organic solvents. It combines readily with the alkyl halides. H. Decker (Ber., 1905, 38, p. 1144) has found that many ortho substituted quinolines will not combine with methyl Iodide owing to steric hindrance, but the difficulty can be overcome in most cases by using methyl sulphate and heating the reaction components to 100 C. for half an hour. Nitric acid and chromic acid have little action on quinoline, but alkaline potassium permanganate oxidizes it to carbon dioxide, ammonia, oxalic, and quinolinic acids (S. Hoogewerif and W. A. v. Dorp,