HCID 22499237, compound → HCID 54392747, compound
Reaction equation
C[C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:10][O:9]2)=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[CH2:14]([NH:21][C:22]1([CH3:33])[CH2:30][C:29]2[C:24](=[CH:25][C:26]([CH3:32])=[C:27]([CH3:31])[CH:28]=2)[CH2:23]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[CH2:8]([O:9][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([OH:9])[CH2:10][N:21]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:22]2([CH3:33])[CH2:30][C:29]3[C:24](=[CH:25][C:26]([CH3:32])=[C:27]([CH3:31])[CH:28]=3)[CH2:23]2)=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12])[C:5]1[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1Participants
3
Conditions
- Temperature
- 110 °C
Procedure
A mixture of 2-(4-methyl-3-nitro-phenyl)-oxirane and benzyl-(2,5,6-trimethyl-indan-2-yl)-amine is heated at 110° C. for 48 hours. The material is used without further purification. ES+ MS m/e 538 (MH+)
Workup
- customThe material is used without further purification
Sources & evidence
- ORD record
- ord-5a88b4e411d44618a80b2458d9c0ceea
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08436017B2
Reaction notes
Loading…