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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541708Generated: October 31, 2026

4-Cyanobenzenesulfonyl chloride → HCID 86636229, compound

https://huagongshe.com/reaction/541708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
ReactantN-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-piperidin-4-ylacetamide tris(trifluoroacetate)HCID 86636131—
ProductHCID 86636229HCID 8663622922%

Reaction Steps

The desired compound was prepared according to the procedure of Example A42 using N-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-piperidin-4-ylacetamide tris(trifluoroacetate) and 4-cyanobenzenesulfonyl chloride as starting materials in 22% yield. LCMS for C31H30ClN8O3S (M+H)+: m/z=629.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-77709e4f53d5418cb26d775de0cbd067
Source noteuspto-grants-2014_10