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HRID 1088770作成日:2026年10月25日

Sodium cyanoborohydride → N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide

https://huagongshe.com/reaction/1088770

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium cyanoborohydrideHCID 5003444—
反応物N-DesesethylzaleplonHCID 9993635—
反応物N-[3-(3-Dimethylaminoacryloyl)phenyl]acetamideHCID 53412415—
反応物HCID 178510443HCID 178510443—
溶媒Acetic AcidHCID 176—
生成物N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamideHCID 136093204—

反応手順

A mixture of 7.0 g of 3'-actamido-3-(N,N-dimethylamino)acrylophenone and 3.3 g. of 3-amino-4-cyanopyrazole in 100 ml of acetic acid was heated at reflux for 8 hours. Crystals that formed on cooling were filtered and dried to give 7.4 g. of N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide, m.p. 254°-256° C. This was reacted with 14.8 g of sodium cyanoborohydride in 50 ml of acetic acid to give 3.0 g of N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide, m.p. 251°-254° C. This is reacted with chloroacetic anhydride and sodium carbonate in toluene as in Example 3 to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04963553
出典データセットuspto-grants-1990_10
ORD IDord-e67bc60cd31343499de30b5df7deaa03
出典メモuspto-grants-1990_10