(1-methyl-1H-indol-5-yl)methylamine → HCID 66837930, compound

HRID 73069

Reaction equation

HRID 73069 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[S:13](Cl)(=[O:15])=[O:14])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH3:17][N:18]1[C:26]2[C:21](=[CH:22][C:23]([CH2:27][NH2:28])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[S:13](=[O:15])(=[O:14])[NH:28][CH2:27][C:23]1[CH:22]=[C:21]2[C:26](=[CH:25][CH:24]=1)[N:18]([CH3:17])[CH:19]=[CH:20]2)[C:5]([O:7][CH2:8][CH3:9])=[O:6]

Participants

3

Reactant 2

HCID 18525752(1-methyl-1H-indol-5-yl)methylamineHCID 86664145Ethyl 3-chloro-4-(chlorosulfonyl)benzoate

Product 1

HCID 66837930HCID 66837930, compound

Procedure

The titled compound was prepared according to the procedure described in step-1 of Example 1 from ethyl 3-chloro-4-(chlorosulfonyl)benzoate and (1-methyl-1H-indol-5-yl)methanamine.

Sources & evidence

ORD record
ord-f2c27c6438ee4fb1bb9e0362b52b15c8
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Linked notes

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