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HRID 2216070作成日:2026年10月27日

Histamine → 4-[5-Bromo-6-[2-(3h-imidazol-4-yl)-ethylamino]-pyridine-3-sulfonyl]-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2216070

反応式

関与物質

役割名称HCID仕込み量
反応物HistamineHCID 774—
反応物TetrahydrofuranHCID 8028—
反応物DiisopropylethylamineHCID 81531—
反応物4-(5-Bromo-6-chloro-pyridine-3-sulfonyl)-5-methylsulfanyl-thiophene-2-carboxylic acid methyl esterHCID 21057179—
溶媒DimethylformamideHCID 6228—
溶媒Dichloromethane methanolHCID 21226129—
生成物4-[5-Bromo-6-[2-(3h-imidazol-4-yl)-ethylamino]-pyridine-3-sulfonyl]-5-methylsulfanyl-thiophene-2-carboxylic acid methyl esterHCID 69586432—

反応手順

The reaction was conducted following the procedure for Example 156: step a, using. 4-(5-bromo-6-chloro-pyridine-3-sulfonyl)-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester (0.050 g, 0.113 mmol), (Example 2: step c), 2-(3H-imidazol-4-yl)-ethylamine (0.027 g, 0.146 mmol), diisopropylethylamine (0.073 g, 0.565 mmol), THF [0.5 mL], DMF [0.5 mL]. Chromatography of the residue (0%–6% MeOH/DCM) yielded the title compound. ESI-MS (m/z): Calcd. for C17H17BrN4O4S3: 518.44 (M+H); found 517.0, 519.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109354B2
出典データセットuspto-grants-2006_09
ORD IDord-45e08faec6ac4092bdc49caed91fa71c
出典メモuspto-grants-2006_09