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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541721Generated: October 28, 2026

2-Fluorobenzenesulphonyl chloride → 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-{1-[(2-fluorophenyl)sulfonyl]piperidin-4-yl}acetamide bis(trifluoroacetate)

https://huagongshe.com/reaction/541721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzenesulphonyl chlorideHCID 137761—
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—
ProductN-[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-{1-[(2-fluorophenyl)sulfonyl]piperidin-4-yl}acetamide bis(trifluoroacetate)HCID 8663624316%

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 2-fluorobenzenesulfonyl chloride as starting materials in 16% yield. LCMS for C30H30ClFN7O3S (M+H)+: m/z=622.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-997f52f3e30f43608505bfb003827ac6
Source noteuspto-grants-2014_10