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HRID 77582作成日:2026年10月25日

Trifluoroacetic acid → HCID 86762769、化合物

https://huagongshe.com/reaction/77582

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物DiisopropylethylamineHCID 81531—
反応物2-Chloro-5-fluoropyrimidineHCID 583466—
反応物HCID 86762770HCID 86762770—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Sodium CarbonateHCID 10340—
生成物HCID 86762769HCID 8676276941%

反応条件

温度50 °C

反応手順

A solution of N-[3-[(4aR,7aS)-2-benzamido-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide; 2,2,2-trifluoroacetic acid (150 mg, 254 μmol), 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is heated in dimethyl sulfoxide (5 mL) overnight at 40° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. for a third night. The reaction is cooled, diluted with saturated aqueous sodium carbonate (50 mL) to give a slurry that is filtered and dried in a vacuum oven at 50° C. for 4 hours to give the title compound (60 mg, 41%). ES/MS (m/e): 449 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841293B1
出典データセットuspto-grants-2014_09
ORD IDord-a8ead401e87b41a0ab024ab02b50ac0d
出典メモuspto-grants-2014_09