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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242972Generated: November 1, 2026

Methyl 2,4-dichloropyrimidine-6-carboxylate → HCID 86618543, compound

https://huagongshe.com/reaction/2242972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2,4-dichloropyrimidine-6-carboxylateHCID 239689—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventDimethylformamideHCID 6228—
ProductHCID 86618543HCID 86618543—

Reaction Steps

A mixture of 2,6-dichloro-pyrimidine-4-carboxylic acid methyl ester (3.98 g, 19.19 mmol, 1.0 equiv; commercially available) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (5.0 g, 24.94 mmol, 1.3 equiv) in anhydrous DMF (100 mL) was heated to 60° C. for 18 h. The organic phase was concentrated under reduced pressure and the crude reaction mixture extracted from a 1 M NaOH (100 mL) solution with ethyl acetate (3×50 mL). The combined organic phases were dried over MgSO4 and the product purified with silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate providing 3.46 g (49%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.42-1.51 (m, 2H), 1.47 (s, 9H), 2.00-2.05 (m, 2H), 2.90-3.01 (m, 2H), 3.92 (s, 3H), 4.05-4.10 (m, 2H), 4.19 (br s, 1H), 7.10 (s, 1H), 7.17 (br s, 1H). 13C NMR (75 MHz, CDCl3): δ28.30, 31.23, 42.41, 48.00, 52.88, 79.61, 106.38, 153.58, 154.61, 161.21, 163.75, 164.23. MS (ISP): 371.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674804B2
Source datasetuspto-grants-2010_03
ORD IDord-3b4b3b64441647bcbe347353a4f8d405
Source noteuspto-grants-2010_03