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【结 构 式】

【分子编号】45225

【品名】2-(tribromomethyl)quinoline

【CA登记号】

【 分 子 式 】C10H6Br3N

【 分 子 量 】379.87638

【元素组成】C 31.62% H 1.59% Br 63.1% N 3.69%

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:(XI)

5)[15N,13C,2H]-Saquinavir: The nitration of [13C6]-benzene (XXI) with [15N]-nitric acid gives the corresponding nitrobenzene (XXII), which is reduced with Sn/HCl to the aniline (XXIII). The cyclization of (XXIII) with crotonic aldehyde (II) by means of ClD/D2O and acetic ahydride yields the tetradeuterated quinoline (XXIV), which is brominated as before givig the tribromo derivative (XXV). The hydrolysis of (XXV) with sulfuric acid as usual affords the [15N,13C6,2H3]-labeled quinoline-2-carboxylic acid (XXVI), which is finally condensed with Ro-32-0445 (VI) by means of HOBT and CDI as indicated.

1 Wiltshire, H.R.; et al.; The synthesis of labelled forms of saquinavir. J Label Compd Radiopharm 1998, 41, 12, 1103.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(II) 22517 (E)-2-butenal 4170-30-3 C4H6O 详情 详情
(VI) 22521 (2S)-N(1)-[(1S,2R)-3-[(3S,4aS,8aS)-3-[(tert-butylamino)carbonyl]octahydro-2(1H)-isoquinolinyl]-1-benzyl-2-hydroxypropyl]-2-aminobutanediamide C28H45N5O4 详情 详情
(XI) 22526 2-(tribromomethyl)quinoline 613-53-6 C10H6Br3N 详情 详情
(XI) 45225 2-(tribromomethyl)quinoline C10H6Br3N 详情 详情
(XII) 14532 2-Quinolinecarboxylic acid; Quinaldic Acid 93-10-7 C10H7NO2 详情 详情
(XII) 45226 2-quinolinecarboxylic acid C10H7NO2 详情 详情
(XXI) 13364 Benzene 71-43-2 C6H6 详情 详情
(XXI) 22536 benzene C6H6 详情 详情
(XXII) 22523 1-nitrobenzene 28250-14-8 C6H5NO2 详情 详情
(XXII) 22537 1-nitrobenzene C6H5NO2 详情 详情
(XXIII) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
(XXIII) 22538 phenylamine; aniline C6H7N 详情 详情
(XXIV) 13161 Quinaldine; 2-Methylquinoline 91-63-4 C10H9N 详情 详情
(XXIV) 45224 2-methylquinoline C10H9N 详情 详情
Extended Information