Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448781생성일: 2026년 10월 25일
L-Methioninol → N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol
https://huagongshe.com/reaction/448781
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | L-Methioninol | HCID 2724404 | — |
| 반응물 | 2-[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one | HCID 57672803 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol | HCID 57672850 | 86% |
반응 단계
100 mg (0.74 mmol) of L-methioninol was added to a solution of 250 mg (0.68 mmol) of 2-[4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one in 20 ml of dimethylformamide. After the mixture was stirred at 80° C. for 15 hours, the reaction solution was concentrated under reduced pressure, ethyl acetate was added thereto, and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, and diisopropyl ether was added to the residue to wash the crystal to obtain 319 mg (86%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08481725B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-fa3326ca2b774c608a65c4913075f958 |
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| 출처 메모 | uspto-grants-2013_07 |
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