化工社化工社 化学情報印刷レポート · 研究参考用
Dichloromethane → 1-Cyclobutyl-4-{[1-(piperidin-1-ylacetyl)azetidin-3-yl]carbonyl}-1,4-diazepane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 1-{[1-(Chloroacetyl)azetidin-3-yl]carbonyl}-4-cyclobutyl-1,4-diazepane | HCID 66739334 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ammonia methanol dichloromethane | HCID 21584172 | — |
| 生成物 | 1-Cyclobutyl-4-{[1-(piperidin-1-ylacetyl)azetidin-3-yl]carbonyl}-1,4-diazepane | HCID 46851319 | 53% |
反応手順
A solution of 1-{[1-(chloroacetyl)azetidin-3-yl]carbonyl}-4-cyclobutyl-1,4-diazepane (40 mg, 0.13 mmol) and piperidine (38 μl, 0.38 mmol) in toluene (2 ml) was heated at 80° C. for 4 hrs in a sealed tube then cooled to RT. The reaction was diluted with DCM (30 ml), washed with a saturated aqueous solution of NaHCO3 (2×15 ml), dried (MgSO4), filtered and concentrated at reduced pressure. The residue was purified by silica FCC (using a gradient of eluents; DCM/MeOH/NH3 99:1:1 to 92:8:1) to give the title compound (25 mg, 53% yield) as a colourless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08912176B2 |
| 出典データセット | uspto-grants-2014_12 |
| ORD ID | ord-d94c01dfbab6401088feab0f042d0515 |
| 出典メモ | uspto-grants-2014_12 |