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HRID 17242作成日:2026年10月26日

Hydrochloric Acid → 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylic acid

https://huagongshe.com/reaction/17242

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物ethyl 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylateHCID 18450882—
溶媒MethanolHCID 887—
生成物2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylic acidHCID 1845055014.8%

反応手順

Ethyl 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylate (433 mg, 0.8018 mmol) in methanol (2 mL) and 2M sodium hydroxide (1.604 mL, 3.207 mmol) was stirred for 23 hours at 50° C., cooled to room temperature and acidified to a pH of 4 with 1M hydrochloric acid. Solids were filtered off and washed with water. The material was purified by HPLC preparative to furnish the title compound as a white solid (61 mg 0.119 mmol): LCMS (Conditions a): MH30 =513 Rt=2.22 minutes; 1H NMR (DMSO-d6, 400 MHz) 9.51 (1 H), 7.99 (1 H), 7.71 (2 H), 7.57 (2 H), 7.34 (2 H), 7.19 (1 H), 7.15 (1 H), 7.07 (1 H), 5.46 (1 H), 4.04 (3 H), 3.91 (3 H), 2.39 (1 H), 1.73 (1 H), 1.46 (1 H), 1.39 (1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737160B2
出典データセットuspto-grants-2010_06
ORD IDord-0a7089297df04bbb97bab492030c82dd
出典メモuspto-grants-2010_06