Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541699Generated: October 31, 2026

4-Cyanobenzoyl chloride → HCID 86636220, compound

https://huagongshe.com/reaction/541699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzoyl chlorideHCID 80172—
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 bis(trifluoroacetate)HCID 86636208—
ProductHCID 86636220HCID 8663622049%

Reaction Steps

The desired compound was prepared according to the procedure of Example A20 using of 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 bis(trifluoroacetate) and 4-cyanobenzoyl chloride as starting materials in 49% yield. LCMS for C32H30ClN8O2 (M+H)+: m/z=593.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-6b051a1ea7d1467cb3b93f71de7c5457
Source noteuspto-grants-2014_10