HCID 68478397, compound → HCID 25212750, compound

HRID 2089607Notes

Reaction equation

HRID 2089607 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH2:11])[CH:10]=1)[NH:7][C:6]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[CH:5]2.[CH3:18][N:19]([CH3:27])[CH:20]([CH2:25][CH3:26])[CH2:21][C:22](=O)[CH3:23]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH:11][CH:23]3[CH2:26][CH2:25][CH:20]([N:19]([CH3:27])[CH3:18])[CH2:21][CH2:22]3)[CH:10]=1)[NH:7][C:6]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[CH:5]2

Participants

3

Reactant 2

HCID 68478397HCID 68478397, compoundHCID 86643835HCID 86643835, compound

Product 1

HCID 25212750HCID 25212750, compound

Procedure

7-Amino-5-chloro-2-phenyl-1H-indole prepared in Example 3 and 4-dimethylaminohexanone were reacted according to the same procedure as Step B of Example 1 to give the title compound.

Sources & evidence

ORD record
ord-c76ff71fa1d84a8484d45f3808c53a35
Source dataset
uspto-grants-2013_05
Patent number
US08436038B2

Reaction notes

Loading…