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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242982Generated: November 2, 2026

Triethylamine → HCID 86618552, compound

https://huagongshe.com/reaction/2242982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantEthyl 2-(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): δ1.19 (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 numberUS07674804B2
Source datasetuspto-grants-2010_03
ORD IDord-65d6a6c158cf4e27a6ded4d1b7a31a5c
Source noteuspto-grants-2010_03