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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541762Generated: November 1, 2026

2-Chlorobenzoyl chloride → 2-Chloro-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]benzamide Hydrochloride

https://huagongshe.com/reaction/541762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
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—
Product2-Chloro-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]benzamide HydrochlorideHCID 6901470824%

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 2-chlorobenzoyl chloride as the starting materials in 24% yield. LCMS for C25H20Cl2N5O (M+H)+: m/z=476.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-c2692589c2d14d9d91bb89c4b18349dd
Source noteuspto-grants-2014_10