Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1753720생성일: 2026년 10월 24일
Oxalyl chloride → 2-methoxy-3-(methylsulfanyl)-N-(1-methyl-1H-tetrazol-5-yl)-4-(trifluoromethyl)benzamide
https://huagongshe.com/ko/reaction/1753720
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | 1-methyl-1H-tetrazol-5-amine | HCID 138492 | — |
| 반응물 | 2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoic acid | HCID 66957907 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 2-methoxy-3-(methylsulfanyl)-N-(1-methyl-1H-tetrazol-5-yl)-4-(trifluoromethyl)benzamide | HCID 89768792 | 46.6% |
반응 단계
1.45 g (98% by weight; 14.3 mmol) of 5-amino-1-methyl-1H-tetrazole were added to 3.00 g (11.3 mmol) of 2-methoxy-3-(methylsulfanyl)-4-(trifluoromethyl)benzoic acid in 30 ml of dry pyridine. 2.00 g (15.8 mmol) of oxalyl chloride were then added, and the mixture was subsequently stirred at room temperature (RT) for three days. Another 500 mg (3.94 mmol) of oxalyl chloride were then added, and the mixture was subsequently stirred at RT for 16 h. For work-up, the contents were substantially freed from the solvent on a rotary evaporator. The residue was stirred with dichloromethane and a saturated solution of sodium bicarbonate. The organic phases were then separated and the organic phase was freed from the solvent on a rotary evaporator. The residue was purified chromatographically, which gave 1.83 g of clean product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09167819B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-6e42f933ffe44b92a03fe1941df17cc5 |
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| 출처 메모 | uspto-grants-2015_10 |
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