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HRID 520450作成日:2026年10月26日

Pyrrolidone carboxylic acid → N-(3-methyl-4-oxo-2-(3-(trifluoromethyl)phenyl)-3,4-dihydroquinazolin-8-yl)-5-oxopyrrolidine-2-carboxamide

https://huagongshe.com/reaction/520450

反応式

関与物質

役割名称HCID仕込み量
反応物Pyrrolidone carboxylic acidHCID 499—
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-oneHCID 58552822—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-(3-methyl-4-oxo-2-(3-(trifluoromethyl)phenyl)-3,4-dihydroquinazolin-8-yl)-5-oxopyrrolidine-2-carboxamideHCID 58552818—

反応手順

Thionylchloride (83 mg, 0.7 mmol) was added to a solution of 5-oxopyrrolidine-2-carboxylic acid 19 (65 mg, 0.5 mmol) in THF (5 mL) at 0° C. DMF (1 drop) was added and the solution was allowed to warm to room temperature for 3 h then cooled to 0° C. A solution of 8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-one 5 (65 mg, 0.2 mmol) and triethylamine (145 mg, 1.44 mmol) in THF (1 mL) was added and the reaction mixture was allowed to warm to room temperature and stirred for 12 h. The reaction mixture was concentrated to dryness and the crude residue was purified by preparative TLC to give Compound 339. MS (ESI) calcd for C21H17F3N4O3: 430.1. found: 431 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326986B2
出典データセットuspto-grants-2016_05
ORD IDord-39b8027fde4f46f28eacddcf04cf7944
出典メモuspto-grants-2016_05