HCID 66837868, compound → HCID 66837935, compound

HRID 73118Notes

Reaction equation

HRID 73118 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:22]2=[N:23][CH:24]=[C:25]([CH2:27][NH2:28])[CH:26]=[C:21]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:25]1[CH:26]=[C:21]2[CH:20]=[CH:19][N:18]([CH3:17])[C:22]2=[N:23][CH:24]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6]

Participants

3

Reactant 2

HCID 66837868HCID 66837868, compoundHCID 86664145Ethyl 3-chloro-4-(chlorosulfonyl)benzoate

Product 1

HCID 66837935HCID 66837935, 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-pyrrolo[2,3-b]pyridin-5-yl)methanamine (step-1 of Example 35).

Sources & evidence

ORD record
ord-4e37f6aadc33490db0e8836e5bbbbf01
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Reaction notes

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