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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175242Generated: October 30, 2026

Glycine methyl ester hydrochloride → Methyl 3-(((5-bromopyridin-2-yl)methoxy)carbonylamino)propanoate

https://huagongshe.com/reaction/2175242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantMethyl 3-aminopropanoate hydrochlorideHCID 2734767—
ReactantMethyl 2-((4-(1-(4-(2,3-dimethylphenoxy)butanoyl)-1,2,3,4-tetrahydroquinolin-5-yl)benzyloxy)carbonylamino)acetateHCID 70982580—
Reactant4-(1-(4-(2,3-Dimethylphenoxy)butanoyl)-1,2,3,4-tetrahydroquinolin-5-yl)benzyl 4-nitrophenyl carbonateHCID 86712581—
Reactant(5-Bromopyridin-2-yl)methyl 4-nitrophenyl carbonateHCID 86712582—
ProductMethyl 3-(((5-bromopyridin-2-yl)methoxy)carbonylamino)propanoateHCID 70981842—

Reaction Steps

The title compound was prepared using a procedure analogous to methyl 2-((4-(1-(4-(2,3-dimethylphenoxy)butanoyl)-1,2,3,4-tetrahydroquinolin-5-yl)benzyloxy)carbonylamino)acetate except that 4-(1-(4-(2,3-dimethylphenoxy)butanoyl)-1,2,3,4-tetrahydroquinolin-5-yl)benzyl 4-nitrophenyl carbonate was replaced with (5-bromopyridin-2-yl)methyl 4-nitrophenyl carbonate and methyl 2-aminoacetate hydrochloride was replaced with methyl 3-aminopropanoate hydrochloride. LCMS, [M+H]+=317.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062028B2
Source datasetuspto-grants-2015_06
ORD IDord-222d4b7824b4438c8710be528572698d
Source noteuspto-grants-2015_06