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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715946Generated: October 29, 2026

tert-butyl (R)-2-[6-bromo-3-bis-(tert-butoxycarbonyl)amino-2-methoxycarbonylphenoxymethyl]pyrrolidine-1-carboxylate → methyl 6-amino-3-bromo-2-((R)-1-pyrrolidin-2-ylmethoxy)benzoate

https://huagongshe.com/reaction/715946

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (R)-2-[6-bromo-3-bis-(tert-butoxycarbonyl)amino-2-methoxycarbonylphenoxymethyl]pyrrolidine-1-carboxylateHCID 71003908—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Productmethyl 6-amino-3-bromo-2-((R)-1-pyrrolidin-2-ylmethoxy)benzoateHCID 86712110100.2%

Reaction Steps

A solution of tert-butyl (R)-2-[6-bromo-3-bis-(tert-butoxycarbonyl)amino-2-methoxycarbonylphenoxymethyl]pyrrolidine-1-carboxylate (Intermediate 8, 3.15 g) in TFA (20 mL) and DCM (20 mL) was stirred at room temperature for 1 hour. The mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate and washed with aqueous potassium carbonate solution. The aqueous layer was extracted with ethyl acetate, dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo to give methyl 6-amino-3-bromo-2-((R)-1-pyrrolidin-2-ylmethoxy)benzoate (1.65 g) as a colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187494B2
Source datasetuspto-grants-2015_11
ORD IDord-602a60a6fd664b14b68823f63885bb2d
Source noteuspto-grants-2015_11