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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542056Generated: November 1, 2026

2-Cyanobenzenesulfonyl Chloride → HCID 86636387, compound

https://huagongshe.com/reaction/542056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyanobenzenesulfonyl ChlorideHCID 522347—
ReactantHCID 86636383HCID 86636383—
ProductHCID 86636387HCID 8663638760%

Reaction Steps

The desired compound was prepared according to the procedure of Example D20, step A, using 6-chloro-N-(2-piperidin-4-ylethyl)-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-amine tetrakis(trifluoroacetate) and 2-cyanobenzenesulfonyl chloride as the starting materials in 60% yield. LCMS for C31H32ClN8O2S (M+H)+: m/z=615.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-9efe68d62df74af29c580025b8a14f70
Source noteuspto-grants-2014_10