2-Thiophenesulfonyl chloride → HCID 25213949, compound

HRID 2089581Notes

Reaction equation

HRID 2089581 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[NH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][C:10]=2[N+:16]([O-])=O.[S:19]1[CH:23]=[CH:22][CH:21]=[C:20]1[S:24](Cl)(=[O:26])=[O:25]>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[NH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][C:10]=2[NH:16][S:24]([C:20]1[S:19][CH:23]=[CH:22][CH:21]=1)(=[O:26])=[O:25]

Participants

3

Reactant 2

HCID 855182-Thiophenesulfonyl chlorideHCID 57901748HCID 57901748, compound

Product 1

HCID 25213949HCID 25213949, compound

Procedure

2-Pyridin-2-yl-7-nitro-1H-indole prepared in Preparation 9 and 2-thiophenesulfonylchloride were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-c6d3cf5b263e4a66ab5a87d6988049dc
Source dataset
uspto-grants-2013_05
Patent number
US08436038B2

Reaction notes

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