Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770844Generated: October 30, 2026

Water → N4-[2-(tert-butylcarbonyl)amino-3-methoxypyrid-6-yl]-2-chloro-5-fluoro-4-pyrimidineamine

https://huagongshe.com/reaction/1770844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
Reactant6-Amino-2-(tert-butylcarbonyl)amino-3-methoxypyridineHCID 57562953—
SolventMethanolHCID 887—
ProductN4-[2-(tert-butylcarbonyl)amino-3-methoxypyrid-6-yl]-2-chloro-5-fluoro-4-pyrimidineamineHCID 57562886—

Reaction Steps

A homogeneous mixture of 6-amino-2-(tert-butylcarbonyl)amino-3-methoxypyridine (35) (1.5 g, 6.72 mmol) and 2,4-dichloro-5-fluoropyrimidine (53) (1.68 g, 10 mmol) in methanol:water (20 mL, each) was stirred at 60° C. for 48 hours. The reaction mixture upon dilution with water (100 mL) gave a solid, which was isolated by filtration to obtain N4-[2-(tert-butylcarbonyl)amino-3-methoxypyrid-6-yl]-2-chloro-5-fluoro-4-pyrimidineamine. LCMS: purity: 89%; MS (m/z): 354 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248190B2
Source datasetuspto-grants-2016_02
ORD IDord-834e7ae56d844d2bb1f7b3e509b5dcd7
Source noteuspto-grants-2016_02