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Chloroacetonitrile → 4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidineacetonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloroacetonitrile | HCID 7856 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine | HCID 19785343 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidineacetonitrile | HCID 19785340 | — |
反応手順
A mixture of 3.22 parts of 2-chloroacetonitrile, 16 parts of 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine, 12.7 parts of sodium carbonate and 225 parts of N,N-dimethylformamide was stirred for 6 hours at room temperature. The reaction mixture was poured onto water. The product was extracted twice with trichloromethane. The combined extracts were dried, filtered and evaporated. The residue was crystallized from acetonitrile. The precipitate was filtered off and the filtrate was evaporated, yielding 16 parts of 4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidineacetonitrile as a residue (compound 147).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05258380 |
| 出典データセット | uspto-grants-1993_11 |
| ORD ID | ord-11da556c18aa4377b1814d5a88123765 |
| 出典メモ | uspto-grants-1993_11 |