HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419722Generated: October 30, 2026
Phosphorus oxychloride → 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine
https://huagongshe.com/reaction/419722
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Allopurinol | HCID 135401907 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine | HCID 221095 | 70.5% |
Reaction Steps
To a solution of allopurinol (20 g, 146.94 mmoles) in toluene (205.71 mL), add phosphoryl chloride (68.27 mL, 734.68 mmoles) and diisopropylethylamine (56.38 mL, 323.26 mmoles) and heat the mixture at 80° C. for 2 hours. Remove the solvent in vacuo to half and pour the mixture into 2 M potassium phosphate, dibasic (734.68 mL, 1.47 moles) in water at 4° C. Stir the mixture overnight at room temperature. Filter off the precipitate through a pad of celite and wash it subsequently with EtOAc. Separate the filtrate, wash the aqueous layer with more EtOAc, join the organic layers, dry it over MgSO4, filter and concentrate in vacuo to afford 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine (16 g, 70.45% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093383B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-2613b7b42af74adc9042866ba3148350 |
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| Source note | uspto-grants-2012_01 |
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