化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → HCID 178482878、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | HCID 178482880 | HCID 178482880 | — |
| 反応物 | HCID 178508386 | HCID 178508386 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178482878 | HCID 178482878 | — |
反応手順
The title compound is synthesized as described for 7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-4,5,6,7-tetrahydro-3H-azepin-2-ylamine (compound 1) from 114 mg of N-methyl-N-(tetrahydro-furan-2-ylmethyl)-4-{2-[2-(7-thioxo-azepan-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridin-6-yl}-benzenesulfonamide (compound A10) and 5.0 ml of methanol containing ammonia (strength: 7.0 M) at 50° C. for 64 hours. Purification by flash chromatography on RP-C8 resin (eluent: acetonitrile/water 2:1 parts by volume) and lyophilization from 1.0 ml of water and 3.0 ml of dioxane afford 14 mg of the title compound as an amorphous, colorless solid of m.p. 260° C. ESI-MS: 511.4 (MH+). TLC: Rf=0.17 (HPTLC RP-C18, acetonitrile/water 2:1 parts by volume).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07790710B2 |
| 出典データセット | uspto-grants-2010_09 |
| ORD ID | ord-b68e71524696419d893c15a8bcc95d53 |
| 出典メモ | uspto-grants-2010_09 |