Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1268137생성일: 2026년 10월 27일
2,4-Hexadienoyl chloride → trans-N-[2-(4-Phenylethynylbenzamido)benzenesulfonyl]-2,4-hexadienamide
https://huagongshe.com/reaction/1268137
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4-Hexadienoyl chloride | HCID 565380 | — |
| 반응물 | 4-Phenylethynyl-N-(2-sulfamoylphenyl)benzamide | HCID 12043043 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | trans-N-[2-(4-Phenylethynylbenzamido)benzenesulfonyl]-2,4-hexadienamide | HCID 86589101 | 48% |
반응 단계
In a stream of nitrogen and at 0° C., 0.10 ml (0.96 mmol) of 2,4-hexadienoyl chloride was added to an anhydrous tetrahydrofuran (10 ml) solution containing 300 mg (0.80 mmol) of 4-phenylethynyl-N-(2-sulfamoylphenyl)benzamide produced in Reference Example 10 and 195 mg (1.60 mmol) of 4-dimethylaminopyridine, the mixture was stirred at room temperature for 1 hour and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with water, a potassium hydrgensulfate aqueous solution and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The thus formed crude crystals were recrystallized from methanol to obtain 180 mg (yield: 48.0%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06555584B1 |
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| 출처 데이터셋 | uspto-grants-2003_04 |
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| ORD ID | ord-b2d1a8e90dff406aa95a2c9993fc90b3 |
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| 출처 메모 | uspto-grants-2003_04 |
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