関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 2-Chloroethyl chloroformate | HCID 12305 | — |
| 反応物 | Vinyl chloroformate | HCID 78808 | — |
| 反応物 | 8-(4-Benzyl-piperazin-1-yl)-6-bromo-quinoline | HCID 18414079 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | 6-Bromo-8-piperazin-1-yl-quinoline | HCID 18414063 | 84% |
反応手順
To a solution of 8-(4-benzyl-piperazin-1-yl)-6-bromo-quinoline (1.6 g, 4.2 mmol) in dichloroethane (50 mL) under a N2 atmosphere was added chloroethylchloroformate (1.26 mL, 12.6 mmol) and the reaction mixture was heated at 80° C. for 4 hours, and at ambient temperaure overnight. No reaction was observed by TLC, therefore vinyl chloroformate (0.35 mL, 6.3 mmol) was added and the reaction was heated at 80° C. for another 4 hours. The cooled reaction was poured into H2O and extracted into CH2Cl2 (2×100 mL) and EtOAc (100 mL). The organic fractions were combined, dried over Na2SO4, and left in EtOAc overnight. The organic layer was concentrated and purified by column chromatography 10%MeOH/CH2C2+NH4OH) affording 1.03 g (84%) of a brown foam. MS(+)APCI m/z 292 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06313126B1 |
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| 出典データセット | uspto-grants-2001_11 |
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| ORD ID | ord-f89bd88f9d2248a5ae5909fa844d6f8d |
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| 出典メモ | uspto-grants-2001_11 |
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