Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1951180생성일: 2026년 10월 27일
Diethyl Ether → 3-{3-[4-Methyl-5-(2-morpholin-4-yl-pyridin-4-yl)-thiazol-2-yl]-ureido}-propionic acid ethyl ester
https://huagongshe.com/reaction/1951180
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Ethyl 3-isocyanatopropanoate | HCID 2733373 | — |
| 반응물 | 4-Methyl-5-(2-morpholin-4-yl-pyridin-4-yl)-thiazol-2-ylamine hydrobromide | HCID 86610328 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-{3-[4-Methyl-5-(2-morpholin-4-yl-pyridin-4-yl)-thiazol-2-yl]-ureido}-propionic acid ethyl ester | HCID 11247129 | — |
반응 단계
To a stirred suspension of 4-Methyl-5-(2-morpholin-4-yl-pyridin-4-yl)-thiazol-2-ylamine hydrobromide (13b) (0.04 g, 0.112 mmol) in DCM (3 ml) is added ethyldiisopropylamine (0.039 ml, 0.224 mmol) to afford a solution. The reaction mixture is then treated with ethyl 3-isocyanatopropionate (0.015 ml, 0.112 mmol) and heated whilst stirring to 60° C. for 5 hours in a sealed reaction vessel. The solution is diluted with DCM and hydrochloric acid (30 ml, 1N HCl) and the layers separated. The aqueous is adjusted to pH 8/9 and extracted with ethyl acetate (3×25 ml). The organics are combined and dried (MgSO4), filtered and concentrated in vacuo to yield a clear oil. Trituration with ether yields the titled compound as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08404684B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-5e87e97a8e9a4e4fa278a906b32701bd |
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| 출처 메모 | uspto-grants-2013_03 |
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