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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967907Generated: October 30, 2026

3-(Chloromethyl)benzoyl chloride → N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-chloromethylbenzamide

https://huagongshe.com/reaction/967907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)benzoyl chlorideHCID 2733324—
ReactantN-(3-amino-4-methylphenyl)-3-morpholinobenzamideHCID 11301391—
ProductN-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-chloromethylbenzamideHCID 2229106198%

Reaction Steps

Using an analogous procedure to that described in Example 63, 3-chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)-3-morpholinobenzamide. There was thus obtained the title compound in 98% yield; NMR Spectrum: (DMSOd6) 2.19 (s, 3H), 3.17 (m, 4H), 3.75 (m, 4H), 4.85 (s, 2H), 7.13 (d, 1H), 7.22 (d, 1H), 7.34 (m, 2H), 7.44 (s, 1H), 7.54 (m, 2H), 7.65 (d, 1H), 7.79 (s, 1H), 7.95 (d, 1H). 8.03 (s, 1H), 9.96 (s, 1H), 10.12 (s, 1H); Mass Spectrum: M+H+ 464.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956037B2
Source datasetuspto-grants-2005_10
ORD IDord-5b5db5023b5247f29e9b6365350ac1fa
Source noteuspto-grants-2005_10