N-cyclopropylsulfamoyl chloride → HCID 68921530、化合物
反応式
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][CH:19]=[CH:18][C:4]=1[CH2:5][NH:6][C:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([NH2:17])[CH:13]=2)[N:8]=1.[CH:22]1([NH:25][S:26](Cl)(=[O:28])=[O:27])[CH2:24][CH2:23]1>N1C=CC=CC=1>[CH:22]1([NH:25][S:26]([NH:17][C:12]2[CH:13]=[C:14]3[C:9](=[CH:10][CH:11]=2)[N:8]=[C:7]([NH:6][CH2:5][C:4]2[CH:18]=[CH:19][CH:20]=[CH:21][C:3]=2[O:2][CH3:1])[CH:16]=[CH:15]3)(=[O:28])=[O:27])[CH2:24][CH2:23]1参加物
4
実験手順
N2-(2-Methoxy-benzyl)-quinoline-2,6-diamine (example 10, step B, 40 mg, 0.143 mmol) was dissolved in 1 mL pyridine. Cyclopropylsulfamoyl chloride (29 mg, 0.186 mmol) was added and the reaction mixture was stirred at room temperature overnight. The solvent was evaporated off and the residue purified by flash chromatography on silica gel (heptane/ethyl acetate 90:10→34:66 gradient). The title compound was obtained as a yellow solid (22 mg, 39%), MS: m/e=397.5 (M+H+).
後処理
- customThe solvent was evaporated off
- customthe residue purified by flash chromatography on silica gel (heptane/ethyl acetate 90:10→34:66 gradient)
出典と根拠
- ORDレコード
- ord-9e1d275f73bd451cac7ee3b7db328294
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08350028B2
反応ノート
読み込み中…