HCID 13823329, compound → 1-(2-Amino-4-methoxyphenyl)indoline
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:11][CH2:10]2)=[C:5]([N+:18]([O-])=O)[CH:4]=1.Cl.NC1C=C(OC)C=CC=1N1C2C(=CC=CC=2)CC1>>[NH2:18][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[CH:7][C:6]=1[N:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1Participants
3
Procedure
It is predicted that if 1-(4-methoxy-2-nitrophenyl)indoline of Example 9a is employed and treated in the manner of Example 5b that 1-(2-amino-4-methoxyphenyl)indoline hydrochloride will be obtained.
Workup
- customwill be obtained
Sources & evidence
- ORD record
- ord-a26ad74e057d4e9faf7c6c8cf24d8c38
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04761411
Reaction notes
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