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HRID 502551作成日:2026年10月26日

Lithium hydroxide, monohydrate → 6-(2-(Benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinic acid

https://huagongshe.com/reaction/502551

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物Methyl 6-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinateHCID 11856360—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物6-(2-(Benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinic acidHCID 1185636163.3%

反応手順

Methyl 6-(2(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinate (211 mg, 0.6 mmol) was dissolved in a mixture of tetrahydrofuran (5 mL) and water (0.5 mL) and treated with lithium hydroxide monohydrate (100 mg, 2.4 mmol). The reaction mixture was stirred at room temperature overnight. The tetrahydrofuran was removed under vacuum and the residue was diluted with water. Dropwise addition of 50% aqueous hydrochloric acid gave a white solid, which was collected by vacuum filtration and dried to yield 6-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinic acid (130 mg) as a white solid. 1H NMR (300 MHz, CDCl3/DMSO-d6): 9.02 (m, 1H), 8.83 (broad s, 1H), 8.32 (m, 1H), 8.10 (d, 1H), 7.95 (d, 1H), 7.68 (d, 1H), 7.39 (t, 1H), 7.25 (t, 1H), 3.71 ppm (m, 4H). MW=342 confirmed by LC-MS, tr=10.56 min (Method Y) MH+=343

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07776847B2
出典データセットuspto-grants-2010_08
ORD IDord-3b63935ff8884981befffea3d040e5c5
出典メモuspto-grants-2010_08