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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38625생성일: 2026년 10월 25일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 7-{(2E)-4-[tert-Butyl(methyl)amino]but-2-enoyl}-4-[(3-chloro-4-fluorophenyl)amino]-5,6,7,8-tetrahydrothieno[2,3-b:5,4-c']dipyridine-3-carbonitrile

https://huagongshe.com/reaction/38625

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물DiisopropylethylamineHCID 81531—
반응물N-Methyl-tert-butylamineHCID 84552—
반응물4-Bromocrotonic acidHCID 6436411—
반응물4-[(3-Chloro-4-fluorophenyl)amino]-5,6,7,8-tetrahydrothieno[2,3-b:5,4-c']dipyridine-3-carbonitrileHCID 58116928—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물7-{(2E)-4-[tert-Butyl(methyl)amino]but-2-enoyl}-4-[(3-chloro-4-fluorophenyl)amino]-5,6,7,8-tetrahydrothieno[2,3-b:5,4-c']dipyridine-3-carbonitrileHCID 5811695438.1%

반응 단계

(2E)-4-Bromobut-2-enoic acid (100 mg, 0.61 mmol) and tert-butyl methylamine (60 mg, 0.67 mmol) were dissolved in DCM (3.0 mL). DIPEA (94 mg, 0.73 mmol) was added, and the mixture was heated overnight to 50° C. After cooling to rt, the compound of Example 55A (75 mg, 0.21 mmol), DCM (1.0 mL), EDCI (48 mg, 0.25 mmol) and DIPEA (32 mg, 0.25 mmol) were added, and the mixture was stirred at rt overnight. Subsequently, it was diluted with water, and the mixture was extracted three times with DCM. The combined organic layers were dried over sodium sulfate, and the solvent was removed in vacuo. The crude product was purified by preparative HPLC to yield 41 mg (37%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524722B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-f403827c0887475ab55fda7d5929c797
출처 메모uspto-grants-2013_09