HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403412Generated: November 1, 2026
Potassium Carbonate → HCID 86619260, compound
https://huagongshe.com/reaction/2403412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(6-(Bromomethyl)-2-chlorothieno[3,2-d]pyrimidin-4-yl)morpholine | HCID 46180726 | — |
| Reactant | N-Methyl-N-(2-pyrrolidinylmethyl)methanesulfonamide | HCID 66617803 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86619260 | HCID 86619260 | 87.9% |
Reaction Steps
To a mixture of 6-bromomethyl-2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (0.50 g) and N-methyl-N-pyrrolidin-2-ylmethyl-methanesulfonamide (390 mg) in acetonitrile (10 mL) was added potassium carbonate (490 mg). The reaction mixture was heated at 80° C. for 16 h and then allowed to cool to room temperature. The reaction mixture was then partitioned between dichloromethane (20 mL) and saturated aqueous sodium bicarbonate solution (20 mL). The combined organics were washed with brine (30 mL), dried (MgSO4), reduced in vacuo and purified by column chromatography to give N-[1-(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-pyrrolidin-2-ylmethyl]-N-methyl-methanesulfonamide as a pale yellow solid (580 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802670B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-110c0f8e7a2b47358702a960f36a4f97 |
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| Source note | uspto-grants-2014_08 |
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