Indole-3-acetamide → HCID 22556841, compound
Reaction equation
CO[C:3](=[O:18])[C:4]([C:6]1[C:16]2=[C:17]3[C:12](=[CH:13][CH:14]=[CH:15]2)[S:11][CH2:10][CH2:9][N:8]3[CH:7]=1)=O.[NH:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:21]([CH2:28][C:29]([NH2:31])=[O:30])=[CH:20]1>>[C:6]1([C:4]2[C:3](=[O:18])[NH:31][C:29](=[O:30])[C:28]=2[C:21]2[C:22]3[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=3)[NH:19][CH:20]=2)[C:16]2=[C:17]3[C:12](=[CH:13][CH:14]=[CH:15]2)[S:11][CH2:10][CH2:9][N:8]3[CH:7]=1Participants
3
Procedure
Beginning with (3,4-dihydro-5-thia-2a-aza-acenaphthylen-1-yl)oxoacetic acid methyl ester and (indol-3-yl)acetamide, the title compound was prepared essentially as described in Example 1.
Sources & evidence
- ORD record
- ord-d7d8b5d4406b4811941a92138dfdbc75
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867198B2
Reaction notes
Loading…