Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055037Generated: October 30, 2026

Water → methyl (3R)-3-[(2-chloro-5-fluoropyrimidin-4-yl)amino]-4,4-dimethylpentanoate

https://huagongshe.com/reaction/1055037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
Reactant(R)-1-methoxy-4,4-dimethyl-1-oxopentan-3-aminium chlorideHCID 86714730—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Productmethyl (3R)-3-[(2-chloro-5-fluoropyrimidin-4-yl)amino]-4,4-dimethylpentanoateHCID 86714731—

Reaction Conditions

Temperature55 °C

Reaction Steps

(R)-1-methoxy-4,4-dimethyl-1-oxopentan-3-aminium chloride, 5a, (37 g, 189 mmol) was dissolved in a mixture of tetrahydrofuran (667 mL) and EtOH (74 mL). The solution was cooled in an ice bath. 2,4-dichloro-5-fluoro-pyrimidine (35 g, 208 mmol) was added, followed by the dropwise addition of triethylamine (85 mL, 606 mmol). The reaction mixture was heated at 55° C. for 17 h. The reaction mixture was then cooled to room temperature after which water (625 mL) and dichloromethane (625 mL) were added. The phases were separated and the aqueous layer was washed with dichloromethane (625 mL). The organic layers were combined and washed with brine. The solvents were removed and the residue was purified on silica gel (EtOAc/Hexanes): LCMS Gradient 10-90%, 0.1% formic acid, 5 min, C18/ACN, RT=3.10 minutes (M+H) 291.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394302B2
Source datasetuspto-grants-2016_07
ORD IDord-d25a1ae188d04b3eada7f5fb82f57f76
Source noteuspto-grants-2016_07