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HRID 82092作成日:2026年10月24日

Acetic Acid → Formate

https://huagongshe.com/ja/reaction/82092

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Sodium triacetoxyborohydrideHCID 5049666—
反応物Azetidine hydrochlorideHCID 12308726—
反応物2-(3-formylphenyl)-N-{5-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-3-yl}acetamideHCID 86672072—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物FormateHCID 283—
生成物2-[3-(azetidin-1-ylmethyl)phenyl]-N-{5-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-3-yl}acetamide formate saltHCID 70817277—

反応手順

Azetidine hydrochloride (10 mg, 0.11 mmol) was added to a stirred solution of 2-(3-formylphenyl)-N-{5-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-3-yl}acetamide (Preparation 192, 23 mg, 0.05 mmol) in DCM (1 mL) and acetic acid (0.04 mL, 0.60 mmol). The reaction mixture was stirred for 30 min at room temperature before addition of sodium triacetoxyborohydride (29 mg, 0.14 mmol) and stirring continued for 3 hours. Water (1 mL) was added and the mixture concentrated in vacuo (with toluene azeotroping). The residue was purified by preparative HPLC to afford the title compound as a formate salt in 12% yield, 3.4 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846698B2
出典データセットuspto-grants-2014_09
ORD IDord-d2d80c6da06f4393a1275495ee8ff960
出典メモuspto-grants-2014_09