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HRID 751577作成日:2026年10月26日

Triethylamine → N-[(1S,1aR,7bR)-4,7-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-1-yl]-N'-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]urea

https://huagongshe.com/reaction/751577

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Amino-4-(4-chlorophenyl)thiazoleHCID 73241—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物(1S,1aR,7bS)-4,7-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-1-carboxylic acidHCID 21304923—
溶媒TolueneHCID 1140—
生成物N-[(1S,1aR,7bR)-4,7-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-1-yl]-N'-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]ureaHCID 60077521—

反応条件

温度110 °C

反応手順

(1S,1aR,7bS)-4,7-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-1-carboxylic acid (50 mg, 0.22 mmol, ee ˜90%) was mixed with toluene (1 ml), triethylamine (0.034 ml, 1.1 eq), 2-amino-4-(4-chlorophenyl)-1,3-thiazole (52 mg, 1.1 eq), DPPA (0.054 ml, 1.1 eq). The reaction mixture was then heated at stirring at 110° C. for 3 h. The reaction mixture was concentrated by rotary evaporation and the product was crystallized from ethanol and collected by filtration to give 50 mg of the product as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405310B2
出典データセットuspto-grants-2008_07
ORD IDord-2d14dd30c2a74be1b7d671bd50de249c
出典メモuspto-grants-2008_07