Methylamine hydrochloride → HCID 66747062, compound
Reaction equation
[C:1]([C:3]1[C:18]([N+:19]([O-:21])=[O:20])=[CH:17][CH:16]=[CH:15][C:4]=1[O:5][CH:6]1[CH2:11][CH2:10][CH:9]([C:12]([OH:14])=O)[CH2:8][CH2:7]1)#[N:2].Cl.[CH3:23][NH2:24]>>[C:1]([C:3]1[C:18]([N+:19]([O-:21])=[O:20])=[CH:17][CH:16]=[CH:15][C:4]=1[O:5][CH:6]1[CH2:7][CH2:8][CH:9]([C:12]([NH:24][CH3:23])=[O:14])[CH2:10][CH2:11]1)#[N:2]Participants
3
Procedure
Prepared as in Example Da from 4-(2-cyano-3-nitrophenoxy)cyclohexanecarboxylic acid (Example 22d) and methylamine hydrochloride as an orange solid (80%). MS 304 (MH+).
Sources & evidence
- ORD record
- ord-6fa2351f287c422aa694fb4c89476907
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815956B2
Reaction notes
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