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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541765Generated: October 31, 2026

Cyclobutanecarbonyl chloride → 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]cyclobutanecarboxamide Hydrochloride

https://huagongshe.com/reaction/541765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanecarbonyl chlorideHCID 78705—
Reactant6-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-amine DihydrochlorideHCID 66896050—
ProductN-[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]cyclobutanecarboxamide HydrochlorideHCID 8663625240%

Reaction Steps

The desired compound was prepared according to the procedure of Example B26, using 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-amine dihydrochloride and cyclobutanecarboxylic acid chloride as the starting materials in 40% yield. LCMS for C23H23ClN5O (M+H)+: m/z=420.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-6d78b2f5a1d0441c8001129731d5ceda
Source noteuspto-grants-2014_10