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【结 构 式】

【分子编号】39274

【品名】1-(4-pyridinyl)piperazine

【CA登记号】1008-91-9

【 分 子 式 】C9H13N3

【 分 子 量 】163.22244

【元素组成】C 66.23% H 8.03% N 25.74%

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:(VIII)

Coupling of Nalpha-Cbz-Nepsilon-Boc-L-lysine (VII) with N-(4-pyridinyl)piperazine (VIII) using TBTU and HOBt afforded amide (IX). After deprotection of the carbobenzoxy group by of (IX) hydrogenation over Pd/C, the resulting amino derivative (X) was coupled with N-Fmoc-3,5-dibromo-D-tyrosine (XI) to furnish the protected dipeptide amide (XII). Removal of the Fmoc protecting group of (XII) was then achieved by treatment with diethylamine in hot MeOH yielding (XIII). After treatment of piperidinyl oxoquinazoline (VI) with carbonyl ditriazole, the resulting intermediate was coupled with amine (XIII) to produce urea (XIV). Finally, removal of the Boc group of (XIV) using trifluoroacetic acid provided the title compound.

1 Eberlein, W.; Wienen, W.; Doods, H.; Rudolf, K.; Entzeroth, M.; Pieper, H.; Engel, W.; Hallermayer, G. (Dr. Karl Thomae GmbH); Modified aminoacids, pharmaceuticals containing these cpds. and methods for their production. JP 2000505100; WO 9811128 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VII) 39273 (2S)-2-[[(benzyloxy)carbonyl]amino]-6-[(tert-butoxycarbonyl)amino]hexanoic acid C19H28N2O6 详情 详情
(VIII) 39274 1-(4-pyridinyl)piperazine 1008-91-9 C9H13N3 详情 详情
(IX) 39275 benzyl (1S)-5-[(tert-butoxycarbonyl)amino]-1-[[4-(4-pyridinyl)-1-piperazinyl]carbonyl]pentylcarbamate C28H39N5O5 详情 详情
(X) 39276 tert-butyl (5S)-5-amino-6-oxo-6-[4-(4-pyridinyl)-1-piperazinyl]hexylcarbamate C20H33N5O3 详情 详情
(XI) 39277 (2R)-3-(3,5-dibromo-4-hydroxyphenyl)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]propionic acid C24H19Br2NO5 详情 详情
(XII) 39278 9H-fluoren-9-ylmethyl (1R)-2-[((1S)-5-[(tert-butoxycarbonyl)amino]-1-[[4-(4-pyridinyl)-1-piperazinyl]carbonyl]pentyl)amino]-1-(3,5-dibromo-4-hydroxybenzyl)-2-oxoethylcarbamate C44H50Br2N6O7 详情 详情
(XIII) 39279 tert-butyl (5S)-5-[[(2R)-2-amino-3-(3,5-dibromo-4-hydroxyphenyl)propanoyl]amino]-6-oxo-6-[4-(4-pyridinyl)-1-piperazinyl]hexylcarbamate C29H40Br2N6O5 详情 详情
(XIV) 39272 3-(4-piperidinyl)-3,4-dihydro-2(1H)-quinazolinone C13H17N3O 详情 详情
(XV) 39280 tert-butyl (5S)-5-([(2R)-3-(3,5-dibromo-4-hydroxyphenyl)-2-[([4-[2-oxo-1,4-dihydro-3(2H)-quinazolinyl]-1-piperidinyl]carbonyl)amino]propanoyl]amino)-6-oxo-6-[4-(4-pyridinyl)-1-piperazinyl]hexylcarbamate C43H55Br2N9O7 详情 详情
Extended Information