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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 916788생성일: 2026년 10월 27일

Acetaldehyde → 1-{3-[4-Amino-7-(1-ethyl-piperidin-4-yl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl]-phenyl}-3-(3,5-dichloro-phenyl)-urea

https://huagongshe.com/reaction/916788

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참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-[3-(4-Amino-7-piperidin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-3-(3,5-dichloro-phenyl)-ureaHCID 67219862—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물1-{3-[4-Amino-7-(1-ethyl-piperidin-4-yl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl]-phenyl}-3-(3,5-dichloro-phenyl)-ureaHCID 6722043310.5%

반응 단계

A solution of 1-[3-(4-Amino-7-piperidin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-3-(3,5-dichloro-phenyl)-urea (100 mg, 0.19 mmol) and acetaldehyde (8.4 mg, 0.19 mmol) in DMF/THF (20%, 10 mL) was stirred for 30 minutes at room temperature. Sodium triacetoxyborohydride (61 mg, 0.29 mmol) was added to the reaction mixture, stirred for 3.5 hours, and concentrated in vacuo. Purification by reverse phase preparative HPLC (HPLC method 2) provided the title compound as a white solid (11 mg, 10%). MS: 553.5 (MH+); HPLC Rf: 1.7 min. (HPLC method 2); HPLC purity: 100%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07271262B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-954eba2bdeda4fa7bcacefd67edd5c6b
출처 메모uspto-grants-2007_09