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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542018Generated: October 25, 2026

2-Isocyanatobenzonitrile → 4-(2-{[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]oxy}ethyl)-N-(2-cyanophenyl)piperidine-1-carboxamide bis(trifluoroacetate)

https://huagongshe.com/reaction/542018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IsocyanatobenzonitrileHCID 2735873—
Reactant6-Chloro-12-(2-piperidin-4-ylethoxy)-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-nonaene tris(trifluoroacetate)HCID 86636347—
Product4-(2-{[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]oxy}ethyl)-N-(2-cyanophenyl)piperidine-1-carboxamide bis(trifluoroacetate)HCID 8663635840%

Reaction Steps

The desired compound was prepared according to the procedure of Example D41 using 6-chloro-12-(2-piperidin-4-ylethoxy)-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-nonaene tris(trifluoroacetate) and 2-isocyanatobenzonitrile as the starting materials in 40% yield. LCMS for C32H32ClN8O2 (M+H)+: m/z=595.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-8680e9f07ac145c0998d8b975e0df94c
Source noteuspto-grants-2014_10