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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541606Generated: October 30, 2026

Benzoyl chloride → HCID 69014435, compound

https://huagongshe.com/reaction/541606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 86636141HCID 86636141—
ProductHCID 69014435HCID 6901443558%

Reaction Steps

The desired compound was prepared according to the procedure of Example A20, using N-[6-chloro-2,4,8,22-tetraazatetracyclo[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 bis(trifluoroacetate) and benzoyl chloride as starting materials in 58% yield. LCMS for C32H32ClN6O2 (M+H)+: m/z=567.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-6e1868b391704a33bb49fff8b89aaff4
Source noteuspto-grants-2014_10