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HRID 471051作成日:2026年10月26日

Triethylamine → Tert-butyl 2,2-difluoro-4-(5-methylthiophene-2-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/471051

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Methylthiophene-2-carboxylic acidHCID 74713—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物tert-Butyl 2,2-difluoro-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989014—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 2,2-difluoro-4-(5-methylthiophene-2-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989071—

反応条件

温度20 °C

反応手順

HATU (0.541 g) was added in one portion to a stirred solution at 0° C. of tert-butyl 2,2-difluoro-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate (example 37, step c) (0.32 g) and 5-methylthiophene-2-carboxylic acid (0.171 g) and triethylamine (0.458 mL) in DMF (20 mL). The mixture was then stirred at 20° C. for 7 hours. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography, elution gradient 0.5 to 5% methanol in dichloromethane. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.4 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629271B2
出典データセットuspto-grants-2014_01
ORD IDord-144a35b2a9584e44ac3c53fb58a05a5e
出典メモuspto-grants-2014_01