Tyramine → HCID 58603605, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([C:8]2[CH:9]=[C:10]([CH:27]=[CH:28][CH:29]=2)[CH2:11][N:12]([CH2:25][CH3:26])[CH2:13][CH2:14][CH2:15][NH:16][C:17](=[O:24])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:5]=[CH:4][N:3]=1.[NH2:30][CH2:31][CH2:32][C:33]1[CH:38]=[CH:37][C:36]([OH:39])=[CH:35][CH:34]=1>>[CH2:25]([N:12]([CH2:11][C:10]1[CH:27]=[CH:28][CH:29]=[C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:30][CH2:31][CH2:32][C:33]3[CH:38]=[CH:37][C:36]([OH:39])=[CH:35][CH:34]=3)[N:7]=2)[CH:9]=1)[CH2:13][CH2:14][CH2:15][NH:16][C:17](=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH3:26]Participants
3
Procedure
Intermediate 44 was coupled with tyramine following procedure F. LC-MS showed the product had the expected M+H+ of 510.
Sources & evidence
- ORD record
- ord-237ccfcafb5641cc83b62a290e2ebb9c
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07732444B2
Reaction notes
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