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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 884814생성일: 2026년 10월 27일

2-Bromoethanol → 3-{5-Amino-4-[3-(2-bromo-ethoxy)-benzoyl]-pyrazol-1-yl}-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/884814

반응식

참여 물질

역할이름HCID투입량
반응물2-BromoethanolHCID 10898—
반응물TriphenylphosphineHCID 11776—
반응물Ammonium ChlorideHCID 25517—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물3-[5-amino-4-(3-hydroxy-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methylbenzamideHCID 11245836—
용매TetrahydrofuranHCID 8028—
생성물3-{5-Amino-4-[3-(2-bromo-ethoxy)-benzoyl]-pyrazol-1-yl}-N-cyclopropyl-4-methylbenzamideHCID 5808894659.1%

반응 단계

To a solution of 3-[5-amino-4-(3-hydroxy-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide (472 mg, 1.26 mmol) in THF (dry, 20 mL) at 0° C. was added of 2-bromoethanol (785 mg, 6.3 mmol), PPh3 (1.3 g, 5.04 mmol) and diethyl azodicarboxylate (877 mg, 5.04 mmol) and the mixture was stirred at room temperature for 72 h. An aqueous solution of NH4Cl was added then the THF layer was isolated. The aqueous layer was extracted by EtOAc. The combined organic phase was washed by brine, purified by preparatory HPLC, to provide the product as a white solid (360 mg, 59%). HPLC (4 minute 10-90 gradient) tR 2.72 min; MS m/z 483.14/485.09 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242117B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-9c8515fca8464af9af822e4292aa122e
출처 메모uspto-grants-2012_08