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HRID 1913384作成日:2026年10月27日

Sulfanilamide → ethyl 5-(4-bromophenyl)-2-methyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/1913384

反応式

関与物質

役割名称HCID仕込み量
反応物SulfanilamideHCID 5333—
反応物Ethyl 2-acetyl-4-(4-bromophenyl)-4-oxobutanoateHCID 14173974—
溶媒Acetic AcidHCID 176—
生成物ethyl 5-(4-bromophenyl)-2-methyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylateHCID 24895703—

反応手順

A mixture of Example 1A (3.3 g, 10.1 mmol) and 4-aminobenzenesulfonamide (1.74 g, 10.1 mmol) in glacial acetic acid (75 mL) was heated to 100° C. for 48 hours. After cooling the mixture was concentrated under reduced pressure. Ether (50 mL) was added to the residue and the precipitate was isolated by filtration. The pale yellow solid was washed with ether and dried. 1H NMR (CDCl3) δ ppm 1.32 (3H), 2.20 (3H), 3.50 (2H), 4.27 (2H), 6.85 (1H), 7.30-7.90 (8H); MS (ESI) m/z m/z 462/464.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609713B2
出典データセットuspto-grants-2013_12
ORD IDord-d7b6c2cac3e140ceafc67beaafe23674
出典メモuspto-grants-2013_12