Azetidine → HCID 86689590, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[C:7]([CH3:12])[CH:8]=[CH:9][CH:10]=2)[C:5]([C:13]([OH:15])=O)=[CH:4][N:3]=1.[NH:16]1[CH2:19][CH2:18][CH2:17]1>>[N:16]1([C:13]([C:5]2[C:6]3[C:11](=[CH:10][CH:9]=[CH:8][C:7]=3[CH3:12])[C:2]([Cl:1])=[N:3][CH:4]=2)=[O:15])[CH2:19][CH2:18][CH2:17]1Participants
3
Procedure
The title compound was prepared by using 1-chloro-5-methylisoquinolin-4-carboxylic acid (Intermediate-10) and azetidine by following the similar procedure as described for intermediate-11a.
Sources & evidence
- ORD record
- ord-af28af46f0b54a87875ae98cd8ed2735
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006442B2
Reaction notes
Loading…