HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364017Generated: October 30, 2026
Ethyl bromoacetate → HCID 66743991, compound
https://huagongshe.com/reaction/2364017
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 66744039 | HCID 66744039 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66743991 | HCID 66743991 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691828B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-784f02052c3240369f31b1e10a5f8d79 |
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| Source note | uspto-grants-2014_04 |
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