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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371457Generated: October 25, 2026

Methanol → 4-({[({[4-(3,4-Dichlorobenzyl)-1,4-oxazepan-2-yl]methyl}amino)carbonyl]amino}methyl)benzamide

https://huagongshe.com/reaction/1371457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-(Aminomethyl)benzamideHCID 2512818—
Reactant[4-(3,4-Dichlorobenzyl)-1,4-oxazepan-2-yl]methylamineHCID 17984703—
SolventDichloromethaneHCID 6344—
Product4-({[({[4-(3,4-Dichlorobenzyl)-1,4-oxazepan-2-yl]methyl}amino)carbonyl]amino}methyl)benzamideHCID 1798471715.8%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a solution of 1,1′-carbonyldiimidazole (0.041 g) in dichloromethane (2 ml) at 0° C. was added dropwise a solution of Intermediate 41 (0.079 g) in dichloromethane (2 ml). The mixture was stirred at 0° C. for 1 h and at 22° C. for 1 h, re-cooled to approximately 0° C. and a solution of 4-aminomethylbenzamide (0.041 g) in a 1:1 mixture of dichloromethane and N,N-dimethylformiamide (4 ml) was added dropwise. The mixture was stirred at 0° C. for 1 h and at 22° C. for 1 h, and applied in two equal portions to ion exchange cartridges (2 g Isolute SCX pre-conditioned with methanol). Elution with methanol (3 column volumes) followed 10% 0.880 ammonia in methanol (2 column volumes) and evaporation of the basic fractions in vacuo gave the crude product. Purification by Biotage flash chromatography on a silica gel cartridge (89), eluting with 150:8:1 dichloromethane/ethanol/0.880 ammonia, gave the title compound as a white solid (0.0186 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157457B2
Source datasetuspto-grants-2007_01
ORD IDord-4497836d24894878a41f9144eb1605bc
Source noteuspto-grants-2007_01