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HRID 234470作成日:2026年10月26日

2-Methyl-4-methoxyaniline → N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamide

https://huagongshe.com/reaction/234470

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-4-methoxyanilineHCID 7610—
反応物N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-methyl-1,3,4-thiadiazol-5-yl)aminocarbonyl]thiophene-3-sulfonamideHCID 10550033—
溶媒PyridineHCID 1049—
生成物N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamideHCID 10646831—

反応手順

N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-methyl-1,3,4-thiadiazol-5-yl)aminocarbonyl]thiophene-3-sulfonamide (EXAMPLE 150), except that 4-methoxy-2-methylaniline was used instead of 2-amino-5-methyl-1,3,4-thiadiazole and that pyridine was not used. The title compound was obtained via HPLC purification as a dull yellow powder (66% yield, m.p. 58°-62° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594021
出典データセットuspto-grants-1997_01
ORD IDord-2858442a5b47413790fae53e184b0f05
出典メモuspto-grants-1997_01