反応式
[CH:1]1([C:4]2[O:5][C:6]3[C:7](=[C:9]([C:28]#[N:29])[C:10]([CH3:27])=[C:11]([C:21]4[CH2:25][CH2:24][CH:23](O)[CH:22]=4)[C:12]=3[N:13]3[CH2:17][CH2:16][C@H:15]([N:18]([CH3:20])[CH3:19])[CH2:14]3)[N:8]=2)[CH2:3][CH2:2]1.Cl.C(O)C>C(O)C.C(OCC)C>[CH:21]1([C:11]2[C:12]([N:13]3[CH2:17][CH2:16][C@H:15]([N:18]([CH3:19])[CH3:20])[CH2:14]3)=[C:6]3[O:5][C:4]([CH:1]4[CH2:2][CH2:3]4)=[N:8][C:7]3=[C:9]([C:28]#[N:29])[C:10]=2[CH3:27])[CH:25]=[CH:24][CH:23]=[CH:22]1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
2-Cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-(3-hydroxycyclopent-1-enyl)-5-methyl-1,3-benzoxazole-4-carbonitrile (I-306) (83 mg, 0.21 mmol) was dissolved in ethanol (0.85 ml) and diethyl ether (1.7 ml), and at room temperature, 1 M hydrochloric acid/ethanol solution (222 μl, 0.22 mmol) was added. After stirring at the same temperature for 4 hours, the solvent was evaporated away under reduced pressure. Ether was added to the residue, and this was concentrated under reduced pressure. This operation was repeated once again. Ether was added to the residue, followed by sonication, and the solvent was removed with a pipette. The residue was dried at 60° C. under reduced pressure for 2 hours to obtain the entitled compound (62 g, 65%) as a brown solid.
後処理
- customthe solvent was evaporated away under reduced pressure
- additionEther was added to the residue
- concentrationthis was concentrated under reduced pressure
- additionEther was added to the residue
- customfollowed by sonication
- customthe solvent was removed with a pipette
- customThe residue was dried at 60° C. under reduced pressure for 2 hours
出典と根拠
- ORDレコード
- ord-86b2c1cb486d4551bdda45bf80d26985
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737166B2
関連ノート
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