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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541722Generated: October 26, 2026

2-(Trifluoromethoxy)benzene-1-sulfonyl chloride → HCID 86636244, compound

https://huagongshe.com/reaction/541722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 2777215—
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 86636244HCID 8663624416%

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-(trifluoromethoxy)benzenesulfonyl chloride as starting materials in 16% yield. LCMS for C31H30ClF3N7O4S (M+H)+: m/z=688.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-f5fb3304ffd44f0991d24a53bec546ae
Source noteuspto-grants-2014_10