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HRID 1766262作成日:2026年10月27日

Sodium Hydroxide → 2,6-Difluorobenzenesulfonic acid 3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1h-indol-5-yl ester

https://huagongshe.com/reaction/1766262

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2,6-Difluorobenzenesulfonyl chlorideHCID 2734271—
反応物3-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indol-5-olHCID 14973207—
溶媒TetrahydrofuranHCID 8028—
生成物2,6-Difluorobenzenesulfonic acid 3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1h-indol-5-yl esterHCID 1022288328.2%

反応手順

By a method similar to Example 31, using a solution of 2,6-difluorobenzenesulfonyl chloride (380 mg, 1.79 mmol) in THF (5 mL) was added to a mixture of 3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-hydroxy-1H-indole (340 mg, 1.49 mmol) in 0.2 N sodium hydroxide (8.2 mL, 1.64 mmol) and THF (5 mL) gave 170 mg (28%) of homogeneous product as a tan solid. The product was crystallized from ethyl acetate to give 96 mg (16%) of the title compound as a yellow powder: mp 183° C. dec; MS(m/e): 405 (M+1), 403 (M−1); Calculated for C20H18F2N2O3S: C, 59.40; H, 4.49; N, 6.93. Found: C, 59.22; H, 4.24; N, 6.65.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07230011B2
出典データセットuspto-grants-2007_06
ORD IDord-f1eda14f4d4a47628ec6d9026a31fc14
出典メモuspto-grants-2007_06