Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257853생성일: 2026년 10월 26일
Dicyclohexylcarbodiimide → N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide
https://huagongshe.com/reaction/257853
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | Dimethyl-1,3-oxazole-5-carboxylic acid | HCID 1132979 | — |
| 반응물 | 4-(4-Ethylthiophenoxy)benzylamine | HCID 117033199 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide | HCID 131718251 | 40.7% |
반응 단계
To a stirred mixture of 2,4-dimethyl-1,3-oxazole-5-carboxylic acid (155 mg, 1.1 mM) and dichloromethane (20 ml) was added 1,3-dicyclohexylcarbodiimide (227 mg, 1.1 mM) at 0°-10° C., and the mixture was stirred for 30 min at the same temperature. To this was added dropwise a solution (10 ml) of 4-(4-ethylthiophenoxy)benzylamine (285 mg, 1.1 mM) in dichloromethane, and the mixture was stirred for 12 h at room temperature. The mixture was poured into ice water, and the mixture was extracted with dichloromethane. The extract was washed with saturated ammonium chloride solution and brine, dried with magnesium sulfate, and concentrated in vacuo. The residue was chromatographed over silica gel to give N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide (164 mg, 39%) as colorless crystals, m.p. 60.0°-64.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05264448 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-9bf5f7adc5fd40939760c7953f06fb16 |
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| 출처 메모 | uspto-grants-1993_11 |
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