2-Aminoindane → HCID 58442370, compound
Reaction equation
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([N:9]2[C:13]([CH3:14])=[CH:12][C:11]([CH3:15])=[N:10]2)[N:3]=1.[NH2:16][CH:17]1[CH2:25][C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18]1>>[Cl:8][C:6]1[N:5]=[C:4]([N:9]2[C:13]([CH3:14])=[CH:12][C:11]([CH3:15])=[N:10]2)[N:3]=[C:2]([NH:16][CH:17]2[CH2:25][C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH2:18]2)[CH:7]=1Participants
3
Procedure
Was prepared according to example 3 from 4,6-dichloro-2-(3,5-dimethyl-pyrazol-1-yl)-pyrimidine and 2-aminoindan.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-edfe908db5004e60aeb4b72558e68d26
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618099B2
Reaction notes
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