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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1024254생성일: 2026년 10월 24일

Acetic Acid → 3,5-dimethyl-4-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-pyrazole-1-carboxylic acid 4-methoxy-benzylamide

https://huagongshe.com/ko/reaction/1024254

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Isocyanic acid, p-methoxybenzyl-HCID 187910—
반응물HCID 59593344HCID 59593344—
용매DichloromethaneHCID 6344—
생성물3,5-dimethyl-4-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-pyrazole-1-carboxylic acid 4-methoxy-benzylamideHCID 24953576—

반응 단계

3-(3,5-dimethyl-1H-pyrazol-4-ylmethyl)-pyrrolo[2,3-b]pyridine-1-carboxylic acid tert-butyl ester (514, 10 mg, 0.03 mmol) was dissolved in dichloromethane (0.5 mL). 1,8-Diazabicylo[5.4.0]unde-7-ene (6 mg, 0.04 mmol) was added. 1-Isocyanatomethyl-4-methoxy-benzene (545, 6.5 mg, 0.04 mmol) was added. The reaction was allowed to proceed at room temperature for 30 minutes. Acetic acid (0.2 mL) was added to the reaction. The solvents were removed under reduced pressure. The residue was dissolved in dimethyl sulfoxide (0.2 mL) and purified by reverse phase HPLC on a Phenomenex column (50 mm×10 mm ID), eluting with water with 0.1% trifluoroacetic acid and 20-100% acetonitrile with 0.1% trifluoroacetic acid over 16 minutes at a flow rate of 6 mL/minute to provide the desired compound P-0135. MS (ESI) [M+H+]+=390.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722702B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-58eb315e9d0c49b1a399d98137485ca3
출처 메모uspto-grants-2014_05