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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426565Generated: October 30, 2026

Triethylamine → HCID 86618552, compound

https://huagongshe.com/reaction/2426565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantEthyl (2,4,6-trichloropyrimidin-5-yl)acetateHCID 27374117—
SolventAcetonitrileHCID 6342—
SolventDimethylacetamideHCID 31374—
ProductHCID 86618552HCID 86618552—

Reaction Steps

A solution of (2,4,6-trichloro-pyrimidin-5-yl)-acetic acid ethyl ester (1.00 g, 3.71 mmol, 1.0 equiv; commercially available from Tyger Scientific Inc, USA), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (1.26 g, 6.31 mmol, 1.7 equiv) and triethylamine (0.77 mL, 0.56 g, 5.57 mmol, 1.5 equiv) in acetonitrile (9 mL) and DMAc (2 mL) was heated by microwave irradiation to 120° 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 0.87 g (54%) of the title compound. 1H NMR (400 MHz, DMSO): δ 1.19 (t, J=8.0 Hz, 3H), 1.35-1.44 (m, 2H), 1.40 (s, 9H), 1.76-1.79 (m, 2H), 2.84 (br s, 2H), 3.73 (s, 2H), 3.93-3.96 (m, 2H), 4.11 (q, J=8.0 Hz, 2H), 4.08-4.13 (m, 1H), 7.52 (d, J=8.0 Hz, 1H). MS (ISP): 433.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968568B2
Source datasetuspto-grants-2011_06
ORD IDord-409f0a53101d4c49bc826ec903bb4160
Source noteuspto-grants-2011_06