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HRID 470949作成日:2026年10月27日

Triethylamine → tert-Butyl 4-(2-methylthiazole-4-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/470949

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Propylphosphonic anhydrideHCID 111923—
反応物2-Methyl-1,3-thiazole-4-carboxylic acidHCID 284728—
反応物Tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochlorideHCID 66964240—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl 4-(2-methylthiazole-4-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989088—

反応手順

1-Propanephosphonic acid cyclic anhydride (1.57M solution in THF, 4.18 mL) was added to a solution of tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (WuXi PharmaTech) (1.92 g), 2-methylthiazole-4-carboxylic acid (0.94 g) and triethylamine (5.48 mL) in DMF (70 mL) and the resulting mixture stirred for 16 h. The reaction mixture was poured into water (500 mL) and extracted with ethyl acetate (3×200 mL). The combined organic solutions were washed with water (2×100 mL) and brine (100 mL), dried over magnesium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with ethyl acetate to give the subtitled compound as a clear oil. Yield 2.30 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-d525b5b5c80547ebbe3364bb93889467
出典メモuspto-grants-2014_01