참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 1-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)piperazin-2-one | HCID 59631389 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | 1,1-Dichloroethane | HCID 6365 | — |
| 생성물 | 1-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)-4-methylpiperazin-2-one | HCID 59631317 | — |
반응 단계
The 1-(4-chloro-5,7-difluoro-3-methylquinolin-2-yl)piperazin-2-one (52.0 mg, 0.167 mmol) and paraformaldehyde (5.01 mg, 0.167 mmol) were dissolved in 1.5 mL of a 2:1 dichloroethane:MeOH solution. The sodium triacetoxyborohydride (106 mg, 0.500 mmol) was added and the reaction mixture was stirred for 6.5 h. The reaction by LCMS had only progressed ˜30%. Some sodium cyanoborohydride (50 mg, 0.796 mmol) was added turning the mixture into a solution again and stirred overnight. The reaction was then diluted with DCM and water. The layers were separated and the organic layer was washed with brine (1×10 mL) and dried over magnesium sulfate to give crude 1-(4-chloro-5,7-difluoro-3-methylquinolin-2-yl)-4-methylpiperazin-2-one. Mass Spectrum (ESI) m/e=312.1 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08940724B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-59238b8b1a8a4eb196186884b4b7af87 |
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| 출처 메모 | uspto-grants-2015_01 |
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