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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872308Generated: October 27, 2026

Methyl 6-amino-5-chloronicotinate → Methyl 6-amino-5-chloronicotinate

https://huagongshe.com/reaction/872308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-amino-5-chloronicotinateHCID 45594319—
Reactanttert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamateHCID 86691038—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-amino-5-chloronicotinateHCID 45594319—
ProductHCID 66665474HCID 66665474—

Reaction Steps

A mixture of 6-amino-5-chloronicotinic acid methyl ester (0.588 g, 3.15 mmol), {1-[4-(2-bromo-2-phenyl-acetyl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester [Int-1-A] (2.00 g, 70% purity by UPLC-MS, 3.15 mmol) and powdered activated 3 Å molecular sieves in isopropanol (9.7 mL) was heated at reflux for 20 hours. On cooling, the mixture was diluted with DCM and water, filtered through Celite and the organic extract washed with brine, dried and concentrated in vacuo. Purification was achieved by chromatography on silica gel (gradient elution: hexane-hexane/ethyl acetate 1:1) to give the title compound contaminated with 6-amino-5-chloronicotinic acid methyl ester. Further purification was achieved by acid extraction of a solution of the crude product in ethyl acetate with dilute aqueous hydrochloric acid (1 M). The organic extract was washed with brine, dried and concentrated in vacuo to give the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975265B2
Source datasetuspto-grants-2015_03
ORD IDord-ef580607d65340f7b466f50e75715fce
Source noteuspto-grants-2015_03