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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1952112생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1952112

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Isocyanic acid, p-methoxybenzyl-HCID 187910—
반응물3-(3,5-Dimethyl-1H-pyrazol-4-ylmethyl)-pyrrolo[2,3-b]pyridine-1-carboxylic acid tert-butyl esterHCID 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 번호US08404700B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-ede87c38e91d43159eb58db9664d3f7e
출처 메모uspto-grants-2013_03