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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158236Generated: November 1, 2026

Ammonia → (4-{4-[2-(Carbamoylmethylamino)ethoxy]phenyl}butyl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1158236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant{2-[4-(4-tert-Butoxycarbonylaminobutyl)phenoxy]ethylamino}acetic acid ethyl esterHCID 58809798—
Product(4-{4-[2-(Carbamoylmethylamino)ethoxy]phenyl}butyl)carbamic acid tert-butyl esterHCID 58809802—

Reaction Steps

A solution of 2 (0.27 g, 0.685 mmol) dissolved in 7 N methanolic ammonia (25 mL) was stirred in a sealed tube at room temperature overnight. After this time, TLC analysis indicated that the reaction was complete. The reaction mixture was concentrated and further dried under vacuum to afford the desired product 3 (0.25 g, quantitative yield) as a yellow viscous oil which was used directly without further purification. m/z (ESI) 366.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807834B2
Source datasetuspto-grants-2010_10
ORD IDord-8f963db03b4d4f1eaa3e5a097370cefb
Source noteuspto-grants-2010_10