反応式
[Cl:1][C:2]1[C:11]2[CH2:10][N:9](CC3C=CC(OC)=CC=3)[C:8](=[O:21])[NH:7][C:6]=2[N:5]=[CH:4][CH:3]=1.C(O)(C(F)(F)F)=O>>[Cl:1][C:2]1[C:11]2[CH2:10][NH:9][C:8](=[O:21])[NH:7][C:6]=2[N:5]=[CH:4][CH:3]=1参加物
3
反応条件
- 温度
- 80 °C
実験手順
1 (90 mg, 0.3 mmol) and TFA (2 mL) were added to a 5 mL sealed tube, and stirred overnight at 80° C. The TFA was removed, and the material was suspended in ether. The resulting precipitate was filtered to provide 3 (56 mg, 99% yield). LC-MS (M+H=184, obsd.=184). 1H NMR: (DMSO-D6) δ 4.37 (s, 2H); 7.03(d, 2H); 7.13 (s, 1H); 8.02 (d, 1H); 9.77 (s, 1H).
後処理
- customsealed tube
- customThe TFA was removed
- filtrationThe resulting precipitate was filtered
出典と根拠
- ORDレコード
- ord-cb41e78705214a389700af2cb0e70cb8
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08569295B2
関連ノート
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