2-(7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indol-9-yl)acetic acid → 2-(7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indol-9-yl)acetamide
反応式
C(OC1C=C(F)C=C2C=1C(CC(N1CC3C(=CC=CC=3)C1)=O)=C[N:13]2CC)C1C=CC=CC=1.[CH2:33]([N:36]1[C:44]2[C:39](=[C:40]3[O:48][CH2:47][CH2:46][O:45][C:41]3=[CH:42][CH:43]=2)[C:38]([CH2:49][C:50]([OH:52])=O)=[CH:37]1)[CH2:34][CH3:35]>>[CH2:33]([N:36]1[C:44]2[C:39](=[C:40]3[O:48][CH2:47][CH2:46][O:45][C:41]3=[CH:42][CH:43]=2)[C:38]([CH2:49][C:50]([NH2:13])=[O:52])=[CH:37]1)[CH2:34][CH3:35]参加物
3
実験手順
Following the procedure (step 1, scheme 31) used to prepare compound 31-2, compound 40-5 gave compound 40-6 in 100% yield as yellow oil. LCMS: calc 274.1 found 275.0 [MH]+.
出典と根拠
- ORDレコード
- ord-bfd21bb846554d219a96d17ea1613b8b
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08912220B2
反応ノート
読み込み中…