戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1024254作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Isocyanic acid, p-methoxybenzyl-HCID 187910—
反応物HCID 59593344HCID 59593344—
溶媒DichloromethaneHCID 6344—
生成物3,5-dimethyl-4-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-pyrazole-1-carboxylic acid 4-methoxy-benzylamideHCID 24953576—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722702B2
出典データセットuspto-grants-2014_05
ORD IDord-58eb315e9d0c49b1a399d98137485ca3
出典メモuspto-grants-2014_05