1(3H)-Isobenzofuranone, 3,3-bis(1-ethyl-2-methyl-1H-indol-3-yl)- → Furo[3,4-b]pyridin-5(7H)-one, 7-[4-(diethylamino)-2-ethoxyphenyl]-7-(1-ethyl-2-methyl-1H-indol-3-yl)-
Reaction equation
[CH2:1]([N:3]([CH2:41][CH3:42])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2([C:20]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[N:22]([CH2:29][CH2:30]CCCCCC)[C:21]=3[CH3:37])[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][N:18]=3)[C:12](=[O:13])[O:11]2)=[C:6]([O:38][CH2:39][CH3:40])[CH:5]=1)[CH3:2].C1(CCNC2C=CC(C3(C4C5C(=CC=CC=5)N(CC)C=4C)C4C(=CC=CN=4)C(=O)O3)=C(OC)C=2)CCCCC1.C(N1C2C(=CC=CC=2)C(C2(C3C4C(=CC=CC=4)N(CC)C=3C)C3C(=CC=CC=3)C(=O)O2)=C1C)C>>[CH2:41]([N:3]([CH2:1][CH3:2])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2([C:20]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[N:22]([CH2:29][CH3:30])[C:21]=3[CH3:37])[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][N:18]=3)[C:12](=[O:13])[O:11]2)=[C:6]([O:38][CH2:39][CH3:40])[CH:5]=1)[CH3:42]Participants
4
Reactant 3
Product 1
Procedure
3-(4-diethylamino-2-ethoxyphenyl)-3-(1-octyl-2-methylindol-3-yl)-4-azaphthalide; 3-(4-cyclohexylethylamino-2-methoxyphenyl)-3-(1-ethyl-2-methylindol-3-yl)-4-azaphthalide; 3,3-bis(1-ethyl-2-methylindol-3-yl)phthalide; 3,6-bis(diethylamino)fluoran-γ-(3′-nitro)anilinolactam; 3,6-bis(diethylamino)fluoran-γ-(4′-nitro)anilinolactam; 1,1-bis[2′,2′,2″,2″-tetrakis(p-dimethylaminophenyl)-ethenyl]-2,2-dinitrileethane; 1,1-bis[2′,2′,2″,2″-tetrakis(p-dimethylaminophenyl)-ethenyl]-2-β-naphthoylethane; 1,1-bis[2′,2′,2″,2″-tetrakis(p-dimethylaminophenyl)ethenyl]-2,2-diacetylethane; bis[2,2,2′,2′-tetrakis(p-dimethylaminophenyl)ethenyl]-methylmalonic acid dimethyl ester.
Sources & evidence
- ORD record
- ord-601196c63ff1464fa980a003ed1e1dbc
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09073376B2
Reaction notes
Loading…