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HRID 18640作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/18640

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US07741364B2
出典データセットuspto-grants-2010_06
ORD IDord-26b8734ec46f438d851b80c723a17934
出典メモuspto-grants-2010_06