Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863생성일: 2026년 10월 23일
Triethylamine → [1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonate
https://huagongshe.com/ko/reaction/863
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate | HCID 140379085 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Ethylacetate heptane | HCID 21899848 | — |
| 생성물 | [1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonate | HCID 140379087 | 50% |
반응 단계
0.7 g (2.53 mmole) (3RS)-1-(N-benzyloxycarbonylamidino)-3-hydroxymethyl pyrrolidine and 0.70 ml (5.05 mmole) triethylamine was dissolved in 15 ml diethyl ether/CH2Cl2 1/1 and the mixture was cooled to 0° C. 0.25 ml (3.29 mmole) methanesulphonyl chloride in 3 ml diethyl ether was slowly added and the reaction mixture was stirred at 0° C for three hours. The solvent was evaporated and the residue was dissolved in ethyl acetate and extracted with a 0.3M KHSO4 -solution. The water layer was washed once with CH2Cl2. The water layer was made neutral with 10M NaOH-solution and extracted twice with CH2Cl2. The combined organic layer was dried (Na2 SO4), filtered and evaporated to yield 0.450 g (50%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723444 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-50d2591cf07947e7ab725904f4df96f4 |
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| 출처 메모 | uspto-grants-1998_03 |
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