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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296562Generated: October 30, 2026

Aniline → [4-(4-Phenylcarbamoylmethoxyphenyl)butyl]carbamic acid benzyl ester

https://huagongshe.com/reaction/1296562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant[4-(4-{[(Benzyloxy)carbonyl]amino}butyl)phenoxy]acetic acidHCID 22054455—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product[4-(4-Phenylcarbamoylmethoxyphenyl)butyl]carbamic acid benzyl esterHCID 2103112599.1%

Reaction Steps

A mixture of [4-(4-benzyloxycarbonylaminobutyl)phenoxy]acetic acid (300 mg, 0.84 mmol), aniline (0.15 mL, 1.70 mmol), DMAP (60 mg, 0.50 mmol) and EDC.HCl (320 mg, 1.70 mmol) in CH2Cl2 (30 mL) was stirred at room temperature for 66 h. The reaction mixture was concentrated under vacuum and the residue was subjected to flash silica gel column chromatography eluting with methanol/CH2Cl2 (1:99, v/v) to give the desired amide 18 as a white solid (360 mg, 99% yield). 1H NMR (300 MHz, CDCl3) δ 1.55 (m, 4H), 2.60 (m, 2H), 3.20 (m, 2H), 4.58 (s, 2H), 4.70 (br s, 1H), 5.10 (s, 2H), 6.88 (d, 2H), 7.15 (m, 31), 7.35 (m, 7H), 7.58 (d, 2H), 8.25 (s, 1H). m/7/z (ESI): 433 [C26H28N2O4+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247637B2
Source datasetuspto-grants-2007_07
ORD IDord-11883f434a6643e28e954e4186f0bcb5
Source noteuspto-grants-2007_07