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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541711Generated: October 26, 2026

Pyridine-3-sulfonyl chloride hydrochloride → 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-(pyridin-3-ylsulfonyl)piperidin-4-yl]acetamide tris(trifluoroacetate)

https://huagongshe.com/reaction/541711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
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-(pyridin-3-ylsulfonyl)piperidin-4-yl]acetamide tris(trifluoroacetate)HCID 8663623231%

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 pyridine-3-sulfonyl chloride hydrochloride as starting materials in 31% yield. LCMS for C29H30ClN8O3S (M+H)+: m/z=605.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-813ca38afda547e3b681e4436eabdf49
Source noteuspto-grants-2014_10