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HRID 1994869作成日:2026年10月26日

Pyridine-2-sulfonyl chloride hydrochloride → ethyl 5-(2-methoxyethoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994869

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine-2-sulfonyl chloride hydrochlorideHCID 13791306—
反応物ethyl 7-amino-5-(2-methoxyethoxy)-1H-indole-2-carboxylateHCID 57476192—
溶媒PyridineHCID 1049—
生成物ethyl 5-(2-methoxyethoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylateHCID 5747620665.2%

反応手順

To a solution of ethyl 7-amino-5-(2-methoxyethoxy)-1H-indole-2-carboxylate (5.80 g) in pyridine (100 mL) was added pyridine-2-sulfonyl chloride monohydrochloride (14.0 g), and the mixture was stirred overnight at room temperature. The solvent was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate. The ethyl acetate layer was washed with 1M hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated brine, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to give the title compound (5.70 g, yield 65%) as a colorless amorphous solid from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). MS: 420 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652133B2
出典データセットuspto-grants-2010_01
ORD IDord-04033fdb7bdd4b48a716582b1957a18a
出典メモuspto-grants-2010_01