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HRID 852621作成日:2026年10月26日

Triethylamine → methyl 4-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-1H-benzimidazole-6-carboxylate

https://huagongshe.com/reaction/852621

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物methyl 4-{[(4-chlorobutyl)sulfonyl]amino}-1H-benzimidazole-6-carboxylateHCID 69360119—
溶媒EthanolHCID 702—
生成物methyl 4-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-1H-benzimidazole-6-carboxylateHCID 6935766025%

反応条件

温度70 °C

反応手順

To a solution of methyl 4-{[(4-chlorobutyl)sulfonyl]amino}-1H-benzimidazole-6-carboxylate (D252) (1 g, 3.23 mmol, 1 equiv) in EtOH (50 ml) was added NEt3 (2 ml, excess) and the resulting solution was stirred at 70° C. for 2 days. then cooled to room temperature and concentrated in vacuo. The residue was dissolved in AcOEt and the organic phase was washed with a 5% aqueous citric acid solution. The aqueous phase was saturated with NaCl and extracted twice with AcOEt. The combined organic phases were dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (CH2Cl2/MeOH: 96/4 to 90/10) gave methyl 4-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-1H-benzimidazole-6-carboxylate (D253) (250 mg, 25%) as a pale yellow solid. [M+H]+=310.3, RT=2.11 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253198B2
出典データセットuspto-grants-2007_08
ORD IDord-18b70689c5024718b1a9b841eacf5174
出典メモuspto-grants-2007_08