関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 反応物 | 7-Morpholinopyrazolo[1,5-a]pyrimidin-5-amine | HCID 58207334 | — |
| 反応物 | 4-(1-(Methoxycarbonyl)cyclopropyl)benzoic acid | HCID 58841109 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | HCID 67064333 | HCID 67064333 | 35% |
反応手順
7-Morpholinopyrazolo[1,5-a]pyrimidin-5-amine (9A, 110 mg, 0.50 mmol) and 4-(1-(methoxycarbonyl)cyclopropyl)benzoic acid (110 mg, 0.50 mmol) were mixed in pyridine (3 ml). TBTU (160 mg, 0.50 mmol) was then added and the mixture was heated to 80° C. for 15 hours. After cooling to room temperature, additional TBTU (53 mg, 0.17 mmol) was added before the heating continued for another 6 hours. After cooling to room temperature, the reaction mixture was quenched with water and was then concentrated to dryness in vacuo. The crude product was purified by preparatory HPLC (35-55% MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white powder (72 mg, 35% yield). 1H NMR (400 MHz, DMSO-d6) δ=11.00 (s, 1 H), 8.10 (d, J=2.3 Hz, 1 H), 7.99 (d, J=8.3 Hz, 2 H), 7.49 (d, J=8.3 Hz, 2 H), 7.41 (s, 1 H), 6.38 (d, J=2.3 Hz, 1 H), 3.88-3.82 (m, 4 H), 3.78-3.70 (m, 4 H), 3.57 (s, 3 H), 1.56-1.50 (m, 2 H), 1.30-1.24 (m, 2 H); ESI-MS: m/z 422.4 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08461163B2 |
|---|
| 出典データセット | uspto-grants-2013_06 |
|---|
| ORD ID | ord-1c8706c46a194e83924b676159e99c3f |
|---|
| 出典メモ | uspto-grants-2013_06 |
|---|