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【结 构 式】

【分子编号】53560

【品名】tert-butyl 4-bromo-2-fluorophenylcarbamate

【CA登记号】n/a

【 分 子 式 】C11H13BrFNO2

【 分 子 量 】290.1321632

【元素组成】C 45.54% H 4.52% Br 27.54% F 6.55% N 4.83% O 11.03%

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:(II)

4-Bromo-2-fluoroaniline (I) was protected as the N-Boc derivative (II) upon treatment with di-tert-butyl dicarbonate. Subsequent palladium-catalyzed bromide displacement in (II) with bis-pinacolatodiborane (III) furnished the arylboronate derivative (IV). The (dioxaspirodecyl)pyrimidine (VII) was prepared by coupling between 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine (V) and 4-hydroxycyclohexanone ethylene ketal (VI) under Mitsunobu conditions. Subsequent Suzuki coupling of iodopyrrolopyrimidine (VII) with boronate (IV) afforded adduct (VIII). Displacement of the 4-chloro of (VIII) with simultaneous N-Boc group cleavage with ammonium hydroxide in dioxan at 120 C in a sealed vessel furnished the diamino compound (IX).

1 Wishart, N.; Barlozzari, T.; Arnold, L.D.; et al.; Structure activity relationships for a novel series of pyrrolo[2,3-d]pyrimidine Tie-2 inhibitors. Proc Am Assoc Cancer Res 2002, 43, Abst 4205.
2 Hirst, G.C.; Ritter, K.; Arnold, L.D.; Wishart, N.; Calderwood, D. (BASF AG); Pyrrolopyrimidines as protein kinase inhibitors. EP 1114053; WO 0017203 .
3 Hirst, G.C.; Rafferty, P.; Arnold, L.D.; Johnston, D.N.; Calderwood, D.; Munschaufer, R. (BASF AG); Pyrrolopyrimidines as tyrosine kinase inhibitors. WO 0172751 .
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) 14723 4-Bromo-2-fluorophenylamine; 4-Bromo-2-fluoroaniline 367-24-8 C6H5BrFN 详情 详情
(II) 53560 tert-butyl 4-bromo-2-fluorophenylcarbamate n/a C11H13BrFNO2 详情 详情
(III) 53561   n/a C12H26B2O4 详情 详情
(IV) 53562 tert-butyl 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate n/a C17H25BFNO4 详情 详情
(V) 53563 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine 123148-78-7 C6H3ClIN3 详情 详情
(VI) 53564 1,4-dioxaspiro[4.5]decan-8-ol 22428-87-1 C8H14O3 详情 详情
(VI) 53565 4-chloro-7-(1,4-dioxaspiro[4.5]dec-8-yl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine n/a C14H15ClIN3O2 详情 详情
(VII) 53566 tert-butyl 4-[4-chloro-7-(1,4-dioxaspiro[4.5]dec-8-yl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-2-fluorophenylcarbamate n/a C25H28ClFN4O4 详情 详情
(VIII) 53567 5-(4-amino-3-fluorophenyl)-7-(1,4-dioxaspiro[4.5]dec-8-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine; 4-[4-amino-7-(1,4-dioxaspiro[4.5]dec-8-yl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-2-fluorophenylamine n/a C20H22FN5O2 详情 详情
Extended Information