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Thonzylamine

Pyrimidines and quinazolines have not been very successful in the antihistamine field. However, thonzylamine (1041 R = OMe) is used in some countries, while its demethoxy-lated analogue, hetramine (1041 R = H), and the quinazoline HPT909 (1042) both have strong support in the literature (63JCS2256, 65AF613, 60MI21301). [Pg.153]

Thiurets — see 1,2,4-Dithiazolidines, diimino-Thonzylamine antihistamine, 3, 153 Thorpe reaction benzothiophenes from, 4, 876 Thorpe-Ziegler cyclization, 2, 74 Three-membered heterocyclic compounds basicity, 7, 23... [Pg.896]

Aromatic rings containing more than one hetero atom also yield active antihistamines. Alkylation of 2-aminopyrimidine (6S) with p-methoxybenzyl chloride gives the corresponding secondary amine (66). Alkylation with the usual chloroamine affords thonzylamine (67), Application of the same sequence to 2-aminothiazole (68) affords zolamine (70). ... [Pg.52]

Pheniramine maleate Phenyltoloxamine Thonzylamine HCI Tibezonium iodide Trimethobenzamide HCI 2otepine... [Pg.1630]

Thiazinone, synthesis, 280 Thiazosulfone, 141 Thiethylperazine, 382 Thiobarbital, 275 Thiofuradene, 231 Thiopental, 274 Thiopropazate, 383 Thioridazine, 389 Thiothixene, 400 Thonzylamine, 52 Thrombosis, 397 Thyroid gland, 95 Thyroxine, 95, 97 Tolazamide, 137 Tolazoline, 241 Tolbutamide, 136 Tolycaine, 17... [Pg.489]

Practically insoluble in water soluble in chloroform. Thonzylamine Hydrochloride... [Pg.1022]

See other pages where Thonzylamine is mentioned: [Pg.437]    [Pg.277]    [Pg.247]    [Pg.1474]    [Pg.1673]    [Pg.1721]    [Pg.1748]    [Pg.169]    [Pg.82]    [Pg.456]    [Pg.1595]    [Pg.621]    [Pg.3216]    [Pg.3216]    [Pg.138]    [Pg.171]    [Pg.196]    [Pg.216]    [Pg.1022]    [Pg.1022]    [Pg.1023]    [Pg.1077]    [Pg.1078]    [Pg.1089]    [Pg.1096]    [Pg.1100]    [Pg.1102]    [Pg.1114]    [Pg.1117]    [Pg.1122]    [Pg.1128]    [Pg.1146]    [Pg.1153]    [Pg.1628]   
See also in sourсe #XX -- [ Pg.52 ]



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Thonzylamine hydrochlorid

Thonzylamine hydrochloride

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