참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Veratrole | HCID 7043 | — |
| 반응물 | 4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl ester | HCID 44203202 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone | HCID 46780868 | — |
반응 단계
A suitable reactor maintained under nitrogen is charged with veratrole (12.5 kg, 90.0 mol) and about 87 kg of tetrahydrofuran. The solution is cooled and maintained below −10° C. while adding n-butyl lithium (22.9 kg, 83.3 mol, 23.3% solution in hexane). The mixture is warmed to about 0° C. for 1 hour, then to about 25° C. for at least 2 hours. In a separate reactor maintained under nitrogen is charged with 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) as a heptanes wet cake (15.6 kg, 57.3 mol, dry weight basis) and about 66 kg of tetrahydrofuran. The mixture is cooled below −10° C.1 and the lithiated veratrole solution is added at such a rate to maintain the temperature below −10° C. The mixture is warmed to about 25° C. for at least 6 hours.2 When complete, the title compound may be utilized in Scheme H, step a, Example 108 as the reaction solution.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713627B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-8c2dc7abec23425880c06c4a583ab511 |
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| 출처 메모 | uspto-grants-2004_03 |
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