Isopropylamine → HCID 21518646, compound
Reaction equation
[OH:1][C:2]1[CH:27]=[CH:26][C:5]([C:6]([C:8]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[O:10][C:9]=2[C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([N+:23]([O-])=O)[CH:18]=2)=[O:7])=[CH:4][CH:3]=1.C(C1OC1)Cl.C(N)(C)C>>[NH2:23][C:19]1[CH:18]=[C:17]([C:9]2[O:10][C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[C:8]=2[C:6](=[O:7])[C:5]2[CH:26]=[CH:27][C:2]([OH:1])=[CH:3][CH:4]=2)[CH:22]=[CH:21][CH:20]=1Participants
4
Procedure
2-(3'-Aminophenyl)-3-(4'-hydroxybenzoyl)benzofuran is prepared by reduction of 3-(4'-hydroxybenzoyl)-2-(3'-nitrophenyl)benzofuran according to the procedure of Example 40. Reaction of this compound with epichlorohydrin followed by ring opening of the resultant epoxy compound with isopropylamine as previously described gives the title compound.
Sources & evidence
- ORD record
- ord-5fb95b50edae457fac96dfb35856d09b
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03975537
Reaction notes
Loading…