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HRID 352851作成日:2026年10月27日

Triethylamine → 1-[(6-tert-Butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine

https://huagongshe.com/reaction/352851

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物PyBOPHCID 2724699—
反応物6-Boc-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-carboxylic acidHCID 22709449—
反応物1-[(6-Chloronaphthalen-2-yl)sulfonyl]-3-ethoxycarbonylpiperazine hydrochlorideHCID 22710075—
溶媒DimethylformamideHCID 6228—
生成物1-[(6-tert-Butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazineHCID 22709517—

反応手順

In N,N-dimethylformamide (30 ml), 6-tert-butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid (WO94/21599) (742 mg), 1-[(6-chloronaphthalen-2-yl)sulfonyl]-3-ethoxycarbonylpiperazine hydrochloride (WO96/10022) (1.00 g) and benzotriazol-1-yloxy-tris(pyrrolidino)phosphonium hexafluorophosphate (PyBOP®) (1.50 g) were dissolved. Triethylamine (0.40 ml) was added to the resulting solution, followed by stirring overnight at room temperature. After the reaction mixture was concentrated under reduced pressure, ethyl acetate was added to the residue. The resulting mixture was washed with water and saturated aqueous NaCl solution and then, dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane ethyl acetate=4:1), whereby the title compound (505 mg, 30%) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747023B1
出典データセットuspto-grants-2004_06
ORD IDord-93559d8da7be42c5ae2bb390dae84e41
出典メモuspto-grants-2004_06