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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367445Generated: October 29, 2026

2-Amino-4,6-dichloropyrimidine → (3S)-1-(2-amino-6-chloro-4-pyrimidinyl)-3-piperidinecarboxylic acid

https://huagongshe.com/reaction/2367445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
ReactantDiisopropylethylamineHCID 81531—
ReactantNipecotic acid, S-(+)-HCID 6575389—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(3S)-1-(2-amino-6-chloro-4-pyrimidinyl)-3-piperidinecarboxylic acidHCID 58504610—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 4,6-dichloro-2-pyrimidinamine (1.397 g, 8.52 mmol), (3S)-3-piperidinecarboxylic acid (1 g, 7.74 mmol) and Hunig's base (2.70 ml, 15.49 mmol) in NMP (10 mL) was heated in the microwave at 140° C. for 90 minutes. LCMS showed mainly desired product. The reaction was cooled down to room temperature, and poured onto water (160 mL). The formed solid was filtered, and the filtered solid was identified as the SM 4,6-dichloro-2-pyrimidinamine. The product stayed in the aqueous solution. 1N HCl was added to adjust the pH=7. Then the aqueous solution was extracted 3× with a mixture of CHCl3 and isopropanol (200:10 mL). The organic layers were combined and evaporated to afford the title compound (1.99 g) as a yellow solid. LC-MS (ES) m/z=257 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-217279fa057d4d6ca6f6942535e06b5c
Source noteuspto-grants-2014_04