HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588985Generated: October 28, 2026
Cesium carbonate → HCID 86665191, compound
https://huagongshe.com/reaction/588985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one | HCID 12095870 | — |
| Reactant | HCID 68749545 | HCID 68749545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86665191 | HCID 86665191 | — |
Reaction Steps
To a solution of tert-butyl 5,6-bis(chloromethyl)pyridine-3-carboxylate (1.80 g, 6.52 mmol) in N,N-dimethylformamide (93.0 mL) was added 4-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (1.80 g, 10.62 mmol), cesium carbonate (3.65 g, 11.21 mmol), and sodium bromide (0.671 g, 6.52 mmol). After 30 min, saturated aqueous sodium bicarbonate was added and the mixture was washed with ethyl acetate (3×). The combined organics were washed with water (3×), brine (3×) and were dried with magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→10% methanol dichloromethane) then a second purification by silica gel chromatography (100% dichloromethane→30% ethyl acetate dichloromethane) gave the title compound as a racemic mixture. Chiral separation of the individual enantiomers was accomplished by use of HPLC using a 10 cm ChiralPak® AD column (60% EtOH hexanes with 0.1% diethylamine) to give the title compound as the 1st eluting enantiomer. MS: m/z=373.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227973B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-696b81b3b8254bcf81c2fe91915f8a28 |
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| Source note | uspto-grants-2016_01 |
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