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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133046생성일: 2026년 10월 26일

Ammonia → 4-[4-(6-Methoxy-pyridin-3-ylmethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-benzoic acid ethyl ester

https://huagongshe.com/reaction/133046

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
반응물(6-Methoxypyridin-3-yl)methanamineHCID 16227379—
반응물4-(4-Chloro-7H-pyrrolo[2,3-D]pyrimidin-6-YL)benzoic acid ethyl esterHCID 23282696—
촉매NickelHCID 935—
용매1-ButanolHCID 263—
용매MethanolHCID 887—
용매TriethylamineHCID 8471—
생성물4-[4-(6-Methoxy-pyridin-3-ylmethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-benzoic acid ethyl esterHCID 69181635—

반응 단계

A mixture of 5.0 g (16.6 mMol) 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)benzoic acid ethyl ester (WO 97/02266) and 2.52 g (18 mMol) of 6-methoxy-pyridin-3-ylmethylamine (CAS: 262295-96-5; prepared from 6-methoxy-nicotin-nitrile by hydrogenation in the presence of Raney-Nickel in methanol containing NH3) in 3.5 ml (25 mMol) of Et3N and 100 ml n-butanol is heated for 8 h to 140° C. Then additional 0.69 g of 6-methoxy-pyridin-3-ylmethylamine and 1.2 ml of Et3N are added. Heating is continued for 6 h and the hot suspension filtrated and the residue washed with n-butanol and hexane to give the title compound; m.p. 305° C.; elemental analysis for C, H, and N, within 0.5% of calculated value.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390805B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-65edb58ab60148a797105c0667e83bed
출처 메모uspto-grants-2008_06