HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516809Generated: October 27, 2026
N,N-Dimethylaniline → 4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amine
https://huagongshe.com/reaction/1516809
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-Deazaguanine | HCID 135408714 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amine | HCID 5324413 | 45.1% |
Reaction Steps
To a solution of 2-amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one (5.00 g, 33.3 mmol), dimethylaniline (4.22 mL, 41.0 mmol) and benzyltriethylammonium chloride (15.2 g, 66.6 mmol) in acetonitrile (25 mL) at room temperature under argon was added POCl3 (18.6 mL, 200 mmol) dropwise for 30 min. The mixture was refluxed at 85° C. for 3 h and cooled to room temperature. The reaction was concentrated in vacuo to brown oil and to the oil was added an ice cold H2O (10 mL). The pH of the solution was adjusted to 5 by the addition of an aqueous NH4OH solution. Silica gel chromatography (CH2Cl2:MeOH=95:5) yielded 2.53 g (45%) of 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine as a light yellow solid. The product was then benzylated at N7 using standard techniques.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227601B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-36a8afe40b29462fabc292d2ce820845 |
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| Source note | uspto-grants-2012_07 |
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