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【结 构 式】

【分子编号】16772

【品名】3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide

【CA登记号】

【 分 子 式 】C14H17N3O

【 分 子 量 】243.3086

【元素组成】C 69.11% H 7.04% N 17.27% O 6.58%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

1) The cyclization of 4-hydrazinobenzonitrile (I) with 4-(benzoyloxy)cyclohexanone (II) in refluxing acetic acid gives 3-(benzoyloxy)-1,2,3,4-tetrahydro-9H-carbazole-6-carbonitrile (III), which is hydrolyzed with aqueous KOH to the corresponding alcohol (IV). The tosylation of (IV) with tosyl chloride in pyridine yields the tosylate (V), which by treatment with methylamine in hot ethanol is converted into 3-(methylamino)-1,2,3,4-tetrahydro-9H-carbazole-6-carbonitrile (VI). The partial hydrolysis of the nitrile group with NaOH/H2O2, with previous protection of the amino group with di-tert-butyl dicarbonate, affords 3-(methylamino)-1,2,3,4-tetrahydro-9H-carbazole-6-carboxamide (VII) as a racemic mixture. The reaction of (VII) with di-tert-butyl dicarbonate gives the carbamate (VIII), which is submitted to chiral HPLC in hexane/ethanol giving the (R)-isomer (IX). Finally, this carbamate is hydrolyzed with aqueous HCl/methanol. 2) The optical resolution can also be performed with the benzoyloxycarbonyl derivative of (VII) in a similar way. 3) The optical resolution of (VII) can also be performed directly with (1S)-(+)-camphorsulfonic acid in methanol. 4) The reaction of cyclohexane-1,4-dione mono 2,2-dimethyltrimethylene ketal (X) with methylamine in toluene gives the corresponding methylimine (XI), which is reduced with H2 over Pd/C in ethanol to the expected methylamine (XII). Finally, this compound is cyclized with 4-aminobenzamide (XIII) by treatment first with NaNO2/HCl and then with sodium dithionite affording the racemic mixture (VII) already described.

1 Graul, A.; Leeson, P.; Castañer, J.; SB-209509/VML-251. Drugs Fut 1997, 22, 7, 725.
2 King, F.D.; Gaster, L.M.; Kaumann, A.J.; Young, R.C. (SmithKline Beecham plc); Use of tetrahydrocarbazole derivs. as 5HT1 receptor agonists. EP 0591280; JP 1994508827; US 5464864; US 5827871; WO 9300086 .
3 Borrett, G.T.; Kitteringham, J.; Porter, R.A.; Shipton, M.R.; Vimal, M.; Young, R.C. (SmithKline Beecham plc); Enantiomers of carbazole derivs. as 5-HT1-like agonists. EP 0674621; JP 1996504790; US 5650426; US 5962501; WO 9414772 .
4 King, F.D.; Gaster, L.M.; Kuamann, A.J.; Young, R.C. (SmithKline Beecham plc); Tetrahydrocarbazole derivs. for the manufacture of a medicament for the treatment of a disease where a 5-HT1-like agonist is indicated. EP 0603432 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 16766 4-hydrazinobenzonitrile C7H7N3 详情 详情
(II) 16767 4-oxocyclohexyl benzoate C13H14O3 详情 详情
(III) 16768 6-cyano-2,3,4,9-tetrahydro-1H-carbazol-3-yl benzoate C20H16N2O2 详情 详情
(IV) 16769 3-hydroxy-2,3,4,9-tetrahydro-1H-carbazole-6-carbonitrile C13H12N2O 详情 详情
(V) 16770 6-cyano-2,3,4,9-tetrahydro-1H-carbazol-3-yl 4-methylbenzenesulfonate C20H18N2O3S 详情 详情
(VI) 16771 3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carbonitrile C14H15N3 详情 详情
(VII) 16772 3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide C14H17N3O 详情 详情
(VIII) 16773 tert-butyl N-[6-(aminocarbonyl)-2,3,4,9-tetrahydro-1H-carbazol-3-yl]-N-methylcarbamate C19H25N3O3 详情 详情
(IX) 16774 tert-butyl N-[(3R)-6-(aminocarbonyl)-2,3,4,9-tetrahydro-1H-carbazol-3-yl]-N-methylcarbamate C19H25N3O3 详情 详情
(X) 16775 3,3-Dimethyl-1,5-dioxaspiro[5.5]undecan-9-one; 1,4-Cyclohexanedione mono-2,2-dimethyltrimethylene ketal 69225-59-8 C11H18O3 详情 详情
(XI) 16776 N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-ylidene)-N-methylamine; N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-ylidene)methanamine C12H21NO2 详情 详情
(XII) 16777 N,3,3-trimethyl-1,5-dioxaspiro[5.5]undecan-9-amine; N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)-N-methylamine C12H23NO2 详情 详情
(XIII) 16778 4-aminobenzamide; p-aminobenzamide 2835-68-9 C7H8N2O 详情 详情
Extended Information