Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773345Generated: October 31, 2026

Diisopropylethylamine → HCID 118483098, compound

https://huagongshe.com/reaction/1773345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantHCID 118483096HCID 118483096—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 118483098HCID 11848309864.6%

Reaction Steps

To a solution of (2,4,5-trichloro-6-oxo-6H-pyrimidin-1-yl)-acetic acid methyl ester (6.0 g, 22.4 mmol) and piperidin-4-yl-carbamic acid tert-butyl ester (4.9 g, 24.4 mmol) in DMF (50 mL) was added DIPEA (5.7 g, 44.3 mmol) dropwise at RT, and the mixture was stirred overnight. The reaction mixture was diluted with water (500 mL), and the solids were collected by filtration. The solids were then dissolved in DCM (100 mL), washed with water (100 mL, 3×), washed with brine (100 mL), dried (Na2SO4) and concentrated. The residue was purified by silica chromatography (1:2 to 1:1, DCM:PE) to give 6.3 g of the title product (64%). 1H NMR (400 MHz, CDCl3): δ 1.22-1.34 (m, 2H), 1.45 (s, 9H), 1.97-2.03 (m, 2H), 2.96-3.09 (m, 2H), 3.68-3.69 (m, 1H), 3.75 (s, 3H), 4.42-4.44 (m, 3H), 4.84 (s, 2H). [M+H] Calc'd for C17H24Cl2N4O5, 435. Found, 435.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255097B2
Source datasetuspto-grants-2016_02
ORD IDord-3ab36978a923415c9e0a9bb016dd14db
Source noteuspto-grants-2016_02