Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53246생성일: 2026년 10월 25일
Sodium Bicarbonate → [1-[2-[(Methylsulphonyl)amino]ethyl]-4-piperidinyl]methyl[2-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamate
https://huagongshe.com/reaction/53246
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)methanesulfonamide | HCID 19962114 | — |
| 반응물 | [2-(3-Methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamoyl Chloride | HCID 19962135 | — |
| 용매 | Toluene ethanol | HCID 21863594 | — |
| 생성물 | [1-[2-[(Methylsulphonyl)amino]ethyl]-4-piperidinyl]methyl[2-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamate | HCID 70079874 | — |
반응 단계
[2-(3-Methyl-1,2,4-oxadiazol-5-yl)phenyl]carbamoyl chloride (7.5 g) was placed in a flask equipped with an air stirrer and ground to a powder N-[2-[4-(Hydroxymethyl)-1-piperidinyl]ethyl]methanesulphonamide (9.33 g) was added and the solids intimately mixed under nitrogen for 10 min at room temperature. The mixture was stirred under a stream of nitrogen at 150° for 10 min. The mixture was allowed to cool then toluene/ethanol (10:1; 110 ml) was cautiously added followed by 8% sodium bicarbonate solution. The mixture was vigorously stirred, the layers were separated and the aqueous phase extracted with 10% ethanol in dichloromethane (4×100 ml). The organic solutions were combined and dried and concentrated in vacuo to give a beige solid. This was purified by FCC eluting with System A (100:8:1) to give the title compound (11.83 g) as fluffy off-white needles.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05618827 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-6d73ce3c728e48c89310726c630ef4b7 |
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| 출처 메모 | uspto-grants-1997_04 |
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