化工社化工社 化学情報印刷レポート · 研究参考用
Sodium Carbonate → 4-Cyano-N-{2-[7-(1-methyl-1H-indol-3-ylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]-ethyl}-benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 1-Methyl-1H-indole-3-carbaldehyde | HCID 87894 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 4-cyano-N-[2-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl)ethyl]-benzenesulfonamide | HCID 68518957 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 生成物 | 4-Cyano-N-{2-[7-(1-methyl-1H-indol-3-ylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]-ethyl}-benzenesulfonamide | HCID 11562043 | 52.8% |
反応手順
A mixture of 4-cyano-N-[2-(9-oxa-3,7-diaza-bicyclo[3.3.1]non-3-yl)-ethyl]-benzenesulfonamide (0.101 g, 0.30 mmol) and 1-methyl-1H-indole-3-carbaldehyde (0.081 g, 0.51 mmol) in 1,2-dichloroethane (4 mL) was agitated for 1.5 hours at room temperature. Sodium triacetoxyborohydride (0.216 g, 1.02 mmol) was added and resulting mixture was agitated over night at room temperature. An aqueous solution of Na2CO3 (3 mL) was added and the aqueous layer was extracted with dichloromethane (3×4 mL). The combined organic layers were concentrated in vacuo and the crude product was purified by chromatography on silica gel using methanol saturated with ammonia in dichloromethane as eluent, which afforded 76 mg (52.8%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07648985B2 |
| 出典データセット | uspto-grants-2010_01 |
| ORD ID | ord-61ae9431537d42e7931650173a6d0410 |
| 出典メモ | uspto-grants-2010_01 |