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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537405Generated: October 29, 2026

1H-indole-4-sulfonyl chloride → N-{3-(2-bromophenyl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}-1H-indole-4-sulfonamide

https://huagongshe.com/reaction/537405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-indole-4-sulfonyl chlorideHCID 55280799—
ReactantTert-butyl{3-(2-bromophenyl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}carbamateHCID 91378583—
ProductN-{3-(2-bromophenyl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}-1H-indole-4-sulfonamideHCID 58504854—

Reaction Steps

Example 67 is subsequently prepared from tert-butyl{3-(2-bromophenyl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}carbamate and indole-4-sulfonyl chloride in the same manner that Example 5 is synthesized. ESI MS Calc. 517.1; Found: 518.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859814B2
Source datasetuspto-grants-2014_10
ORD IDord-c3f8c64bb051402d90c119cbdb44b87d
Source noteuspto-grants-2014_10