Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364017Generated: October 30, 2026

Ethyl bromoacetate → HCID 66743991, compound

https://huagongshe.com/reaction/2364017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantMorpholineHCID 8083—
ReactantSodium hydrideHCID 24758—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 66744039HCID 66744039—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
ProductHCID 66743991HCID 6674399134%

Reaction Steps

To a solution of 6-bromo-3-(4-methoxybenzyl)-2,2-dimethyl-2,3-dihydrothieno[3,2-d]pyrimidin-4(1H)-one (500 mg, 1.31 mmol) in DMF (13 mL) was added NaH (50%, 94 mg, 1.97 mmol) at 0° C. After stirring at room temperature for 15 min, ethyl bromoacetate (0.16 mL, 1.44 mmol) was added at once. After stirring at room temperature for 0.5 h, the mixture was poured into saturated aqueous NaHCO3. The organic materials were extracted with EtOAc. To the aqueous layer was added 1 M HCl until pH 5. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, and then dried over Na2SO4. After removal of the solvent at reduced pressure, the residual brown oil was mixed with N-ethyl-N-(1-methylethyl)propan-2-amine (0.24 mL, 1.37 mmol) and morpholine (0.072 mL, 0.82 mmol) in DMF (5 mL), and HATU (312 mg, 0.82 mmol) was added. After stirring at room temperature for 1 h, water and EtOAc were added to quench the reaction. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (Purif, silica gel, 95:5 hexane-EtOAc to EtOAc) to give a brown oil. After the oil was dissolved in TFA (2 mL), the mixture was stirred at 70° C. for 2 h. After removal of the solvent at reduced pressure, saturated aqueous NaHCO3 was added. The organic materials were extracted with EtOAc. The combined extracts were washed with brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was triturated with EtOAc and collected by filtration to afford the title compound (97 mg) as a brown solid. After concentration of the filtrate, the residue was purified by column chromatography (Purif, silica gel, 95:5 hexane/EtOAc to EtOAc then to 90:10 EtOAc/MeOH) to give the title compound (27 mg) as a brown solid. Total yield of the title compound (97+27 mg) was 27%:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-784f02052c3240369f31b1e10a5f8d79
Source noteuspto-grants-2014_04