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HRID 448781作成日:2026年10月26日
L-Methioninol → N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol
https://huagongshe.com/reaction/448781
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | L-Methioninol | HCID 2724404 | — |
| 反応物 | 2-[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one | HCID 57672803 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol | HCID 57672850 | 86% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08481725B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-fa3326ca2b774c608a65c4913075f958 |
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| 出典メモ | uspto-grants-2013_07 |
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