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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026831생성일: 2026년 10월 26일

2-Fluorobenzoyl chloride → tert-Butyl (2-(7-(2-fluoro-4-(2-fluorobenzamido)phenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

https://huagongshe.com/reaction/1026831

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluorobenzoyl chlorideHCID 9808—
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl (2-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamateHCID 57919490—
용매DichloromethaneHCID 6344—
생성물tert-Butyl (2-(7-(2-fluoro-4-(2-fluorobenzamido)phenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamateHCID 58236607108.3%

반응 단계

To a solution of aniline 46 (300 mg, 0.569 mmol) in DCM (10 mL) at 0° C. was added DIPEA (0.199 mL, 1.137 mmol) and 2-fluorobenzoyl chloride (135 mg, 0.853 mmol) and the suspension was stirred overnight at room temperature. The reaction mixture was concentrated and the residue was partitioned between EtOAc and water. The organic layer was collected, dried and concentrated. The residue was purified using Biotage (eluent EtOAc, 25 g Silicycle HR column) to provide the title compound 356 (400 mg, 0.616 mmol, quantitative yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729268B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-50519c0778dd49eb9497d36d597cc593
출처 메모uspto-grants-2014_05