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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095519Generated: November 1, 2026

Acetic Acid → 4-{2-[(2-tert-Butoxycarbonyl-ethyl)-(3-chloro-4-trifluoromethoxy-phenyl)-amino]-ethylamino}-butyric acid methyl ester

https://huagongshe.com/reaction/2095519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
Reactant4-Aminobutyric acid methyl ester hydrochlorideHCID 2756383—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl esterHCID 86652690—
SolventDichloromethaneHCID 6344—
Product4-{2-[(2-tert-Butoxycarbonyl-ethyl)-(3-chloro-4-trifluoromethoxy-phenyl)-amino]-ethylamino}-butyric acid methyl esterHCID 67074302—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.50 g (1.3 mmol) of 3-[(3-chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl ester in 6 ml dichloromethane was added dropewise to a cooled (0° C., pH ca. 5) suspension of 0.22 g (1.4 mmol) methyl 4-aminobutyrate hydrochloride, 0.18 ml (1.3 mmol) triethylamine, 0.15 ml (2.6 mmol) acetic acid and 0.32 g (1.5 mmol) sodium triacetoxyborohydride in 4 ml of dichloromethane and stirred 30 min at 0° C. The reaction was extracted with aqueous saturated NaHCO3/EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3 and dried over Na2SO4 to yield after evaporation of the solvent 0.61 g (83%) of the titled compound as yellow oil. MS: 483.19 (MH+, Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-be1559557b7e463ea95ac63924b8a4e8
Source noteuspto-grants-2013_05