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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846096Generated: November 3, 2026

N-[4-Methoxy-3-(4-bromophenyl)aminocarbonyl-phenyl]-2-chloro-5-(tert-butoxycarbonylamino)methyl-benzamide → N-[4-Methoxy-3-(4-bromophenyl)aminocarbonyl-phenyl]-2-chloro-5-aminomethyl-benzamide

https://huagongshe.com/reaction/1846096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-Methoxy-3-(4-bromophenyl)aminocarbonyl-phenyl]-2-chloro-5-(tert-butoxycarbonylamino)methyl-benzamideHCID 67116272—
Solvent1,4-DioxaneHCID 31275—
ProductN-[4-Methoxy-3-(4-bromophenyl)aminocarbonyl-phenyl]-2-chloro-5-aminomethyl-benzamideHCID 67116388—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2.66 g N-[4-methoxy-3-(4-bromophenyl)aminocarbonyl-phenyl]-2-chloro-5-(tert.butoxycarbonylamino)methyl-benzamide (4.51 mmol) 25 mL 4M HCl in dioxane and 50 mL dioxane was stirred for 2 h at rt and 60 min at 50° C. and concentrated i.vac. to furnish the subtitle compound. Yield: (quantitative). MS [M+H]+=488 (Br/Cl-isotope pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951999B2
Source datasetuspto-grants-2015_02
ORD IDord-2d845f58350c44959165526c96fb560a
Source noteuspto-grants-2015_02