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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242970Generated: November 1, 2026

4-Chloro-2,6-dimethoxypyrimidine → HCID 67147560, compound

https://huagongshe.com/reaction/2242970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2,6-dimethoxypyrimidineHCID 80600—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventAcetonitrileHCID 6342—
SolventDimethylacetamideHCID 31374—
ProductHCID 67147560HCID 67147560—

Reaction Steps

A solution of 4-chloro-2,6-dimethoxy-pyrimidine (1.92 g, 11.0 mmol, 1.0 equiv; commercially available), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (2.64 g, 13.20 mmol, 1.2 equiv) and N-ethyl diisopropylamine (2.24 mL, 1.71 g, 13.20 mmol, 1.2 equiv) in acetonitrile (8 mL) and DMAc (2 mL) was heated by microwave irradiation to 160° C. for 1 h and then to 180° C. for 30 min. The reaction mixture was concentrated under reduced pressure and the crude material purified by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate providing 1.22 g (33%) of the title compound. 1H NMR (300 MHz, CDCl3): δ1.39-1.48 (m, 2H), 1.46 (s, 9H), 1.97-2.00 (m, 2H), 2.85-2.96 (m, 2H), 3.86 (s, 3H), 3.89 (s, 3H), 3.96-4.02 (m, 3H), 5.52 (d, J=7.9 Hz, 1H). 13C NMR (75 MHz, CDCl3): δ 28.16, 31.48, 42.39, 47.95, 53.12, 53.76, 79.24, 100.51, 154.40, 164.60, 164.99, 171.52. MS (ISP): 339.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674804B2
Source datasetuspto-grants-2010_03
ORD IDord-fb10406e99c24e94bf7628f4df9afa24
Source noteuspto-grants-2010_03