Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170243Generated: November 3, 2026

Potassium Carbonate → HCID 12003796, compound

https://huagongshe.com/reaction/1170243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl N-(2-aminoethyl)carbamate hydrochlorideHCID 12715871—
Reactant4-(7-Fluoro-quinazolin-4-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 59551736—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 12003796HCID 1200379673%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a mixture of 4-(7-fluoro-quinazolin-4-yl)-piperidine-1-carboxylic acid tert-butyl ester (458 mg, 1.38 mmol), which was prepared as described in Example 12b, and (2-amino-ethyl)-carbamic acid benzyl ester hydrochloride (446 mg, 1.93 mmol) in DMSO (1.0 mL) was added K2CO3 (1.52 g, 11.04 mmol). The mixture was stirred at 115° C. overnight and subsequently partitioned between EtOAc and water. The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated. The residue was purified by flash column chromatography on silica gel (EtOAc as eluent) to afford the desired product as a white solid (400 mg, 73%). 1H NMR (CDCl3) δ 9.13 (s, 1H), 8.69 (dd, J=9.40 and 2.35 Hz, 1H), 8.08 (d, J=9.53 Hz, 1H), 7.42 (d, J=2.33 Hz, 1H), 5.25 (br, 1H), 4.31 (m, 2H), 4.09 (t, J=8.21 Hz, 2H), 3.69 (t, J=8.14 Hz, 2H), 3.63 (m, 1H), 2.95 (m, 2H), 1.77-2.04 (4H), 1.48 (s, 9H). Calcd for C21H28N5O3 (MH+) 398.3, found 398.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825244B2
Source datasetuspto-grants-2010_11
ORD IDord-6623a0b603174b0f90675205178eb773
Source noteuspto-grants-2010_11