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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18251Generated: October 27, 2026

Trifluoroacetic acid → Methyl 2-((5-bromopyridin-2-yl)amino)acetate

https://huagongshe.com/reaction/18251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 2-[(5-bromopyridin-2-yl)[(tert-butoxy)carbonyl]amino]acetateHCID 22139000—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-((5-bromopyridin-2-yl)amino)acetateHCID 22139049100.4%

Reaction Steps

A 50% solution of TFA in CH2Cl2 (200 mL) was added to 5-bromo-2-[N-(tert-butoxycarbonyl)-N-(methoxycarbonylmethyl)amino]pyridine (16.5 g, 46 mmole). After stirring for 45 min the reaction was concentrated to dryness, and the residue was diluted with 1.0 N Na2CO3 (300 mL). The mixture was extracted with EtOAc (300 mL), and the organic layer was washed with brine, dried (Na2SO4), and concentrated to dryness under vacuum. The title compound (11.32 g, 100%) was obtained as a white solid: 1H NMR (400 MHz, CDCl3) δ 8.13 (d, J=2.3 Hz, 1 H), 7.48 (dd, 1 H), 6.40 (d, J=8.8 Hz, 1 H), 4.95 (br s, 1 H), 4.12 (d, J=5.5 Hz, 2 H), 3.78 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741339B2
Source datasetuspto-grants-2010_06
ORD IDord-716901cfd6a641bfb97b86e0d3c53f10
Source noteuspto-grants-2010_06