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【结 构 式】

【分子编号】40967

【品名】(3R,8aR)-3-(bromomethyl)-3-methyltetrahydro-1H-pyrrolo[2,1-c][1,4]oxazine-1,4(3H)-dione

【CA登记号】

【 分 子 式 】C9H12BrNO3

【 分 子 量 】262.10322

【元素组成】C 41.24% H 4.61% Br 30.49% N 5.34% O 18.31%

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:(IV)

Coupling of the chiral auxiliary (R)-proline (I) with methacryloyl chloride (II) under Schotten-Baumann conditions provided amide (III). This was converted to bromolactone (IV) by asymmetric bromolactonization in the presence of N-bromosuccinimide. Subsequent acid hydrolysis yielded the chiral (R)-bromoacid (V), that was converted to acid chloride (VI) and then coupled with 4-amino-2-trifluoromethylbenzonitrile (VII) in DMA at low temperature to afford anilide (VIII). Coupling with 4-aminothiophenol (IX) using NaH in THF produced sulfide (X). Finally, conversion of the aniline precursor (X) to the target isothiocyanate was achieved by reaction with thiophosgene in the presence of NaHCO3.

1 Mukherjee, A.; et al.; Affinity labeling of the androgen receptor with nosteroidal chemoaffinity ligands. Biochem Pharmacol 1999, 58, 8, 1259.
2 Dalton, J.T.; Miller, D.D.; Kirkovsky, L.; Mukherjee, A.; Yin, D.; Chiral nonsteroidal affinity ligands for the androgen receptor. 1. Bicalutamide analogues bearing electrophilic groups in the B aromatic ring. J Med Chem 2000, 43, 4, 581.
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) 28284 D-proline 344-25-2 C5H9NO2 详情 详情
(II) 33553 2-methylacryloyl chloride 920-46-7 C4H5ClO 详情 详情
(III) 40972 (2R)-1-methacryloyl-2-pyrrolidinecarboxylic acid C9H13NO3 详情 详情
(IV) 40967 (3R,8aR)-3-(bromomethyl)-3-methyltetrahydro-1H-pyrrolo[2,1-c][1,4]oxazine-1,4(3H)-dione C9H12BrNO3 详情 详情
(V) 40968 (2R)-3-bromo-2-hydroxy-2-methylpropionic acid C4H7BrO3 详情 详情
(VI) 40969 (2R)-3-bromo-2-hydroxy-2-methylpropanoyl chloride C4H6BrClO2 详情 详情
(VII) 18743 4-amino-2-(trifluoromethyl)benzonitrile;5-Amino-2-cyanobenzotrifluoride 654-70-6 C8H5F3N2 详情 详情
(VIII) 40970 (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide C12H10BrF3N2O2 详情 详情
(IX) 16490 4-aminophenylhydrosulfide; 4-aminothiophenol; 4-aminobenzenethiol 1193-02-8 C6H7NS 详情 详情
(X) 40971 (2R)-3-[(4-aminophenyl)sulfanyl]-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide C18H16F3N3O2S 详情 详情
Extended Information