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HRID 560541作成日:2026年10月26日

1,1'-Carbonyldiimidazole → (R)-ethyl 2-(3-(1-hydroxy-3-phenylpropan-2-yl)ureido)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/560541

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Ethyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
反応物phenylalaninol, (R)-HCID 853475—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-ethyl 2-(3-(1-hydroxy-3-phenylpropan-2-yl)ureido)-4-methylthiazole-5-carboxylateHCID 73213189—

反応手順

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (1.86 g, 10.0 mmol) in tetrahydrofuran (50 mL) was added 1,1′-carbonyldiimidazole (1.95 g, 12.0 mmol) at ambient temperature. The resulting reaction mixture was stirred at ambient temperature for 17 hours, followed by the addition of (R)-(+)-2-amino-3-phenyl-1-propanol (2.00 g, 13.2 mmol). The reaction mixture was kept stirring at ambient temperature for 50 hours. The solvent was removed in vacuo. The residue was dissolved in ethyl acetate (200 mL) and washed with water and brine. The organic solution was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to afford the title compound in 88% (3.20 g): MS (ES+) m/z 364.4 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063084B2
出典データセットuspto-grants-2011_11
ORD IDord-0b04c58388994db6a504952ada57d2cb
出典メモuspto-grants-2011_11