4-(2-Thienyl)aniline → HCID 46184607, compound
Reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[NH:8][C:9]1[N:14]=[C:13]([NH:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]3ON=[CH:24][CH:23]=3)=[CH:18][CH:17]=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1.[S:30]1C=CC=[C:31]1C1C=CC(N)=CC=1>>[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[NH:8][C:9]1[N:14]=[C:13]([NH:15][C:16]2[CH:17]=[CH:18][C:19]([C:22]3[S:30][CH:31]=[CH:24][CH:23]=3)=[CH:20][CH:21]=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1Participants
3
Procedure
This compound was synthesised using the synthetic scheme described for the synthesis of compound 122, and using 4-(thiophen-2-yl)aniline in step 1. MS: 410.0 (M+H).
Workup
- customThis compound was synthesised
Sources & evidence
- ORD record
- ord-f4d79ba79b8b4fb8a6c0e5c1673231f9
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318755B2
Reaction notes
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