HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772179Generated: November 3, 2026
Dichloromethane → 4-Chloro-2,5,6,7-tetramethyl-5H-pyrrolo[3,2-d]pyrimidine
https://huagongshe.com/reaction/1772179
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2,5,6,7-Tetramethyl-3H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one | HCID 136030078 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-2,5,6,7-tetramethyl-5H-pyrrolo[3,2-d]pyrimidine | HCID 59939483 | — |
Reaction Steps
A mixture of 2,5,6,7-tetramethyl-3H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one N9b (0.334 g, 1.75 mmol) and POCl3 (4 ml) is stirred at 100° C. for 17 hours. At 0° C. DCM (30 ml) and aqueous sodium hydroxide (1 mol/1, 20 ml) is added under vigorous stirring. The water phase is made basic with an aqueous solution of sodium hydroxide (1 mol/l) and extracted with DCM. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is used without further purification. Yield: 330 mg (90%). HPLC-MS: M+H=210; tR=0.92 min (METHOD—1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249151B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-82c151c0ab304f97af09c059e91f951d |
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| Source note | uspto-grants-2016_02 |
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