HCID 10113742、化合物 → HCID 10136885、化合物
反応式
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[C:14]3[C:15]([CH3:29])=[C:16]([NH:21][C:22]([C:24]4[S:25][CH:26]=[CH:27][CH:28]=4)=O)[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]=3[O:12][C:11]2([CH3:31])[CH3:30])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]>CO>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:10]2[C:14]3[C:15]([CH3:29])=[C:16]([NH:21][CH2:22][C:24]4[S:25][CH:26]=[CH:27][CH:28]=4)[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]=3[O:12][C:11]2([CH3:31])[CH3:30])=[CH:8][CH:9]=1)([CH3:3])[CH3:2]参加物
3
実験手順
By using N-[3-(4-isopropylphenyl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl]-2-thiophenecarboxamide, the title compound was synthesized according to Example 2b. Yield: 61%. Melting point: 101-103° C. (Methanol)
出典と根拠
- ORDレコード
- ord-f9362813cbe04dd1adebe663f97e2397
- 出典データセット
- uspto-grants-2002_11
- 特許番号
- US06479536B1
反応ノート
読み込み中…