Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | 2-Amino-4H-pyrrolo[2,3-d]pyrimidin-4-one | HCID 21904348 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20246378 | HCID 20246378 | 80.1% |
Reaction Steps
2-Aminopyrrolo(2,3-d)pyrimidin-4-one (6.0 g) is suspendeed in pyridine (80 ml) and, with stirring on an ice bath, n-octanoyl chloride (22.8 g) is added. The reaction mixture is warmed at 85° C. for 30 minutes and the solvent is distilled off under reduced pressure. Dilute hydrochloric acid is added to the residue and the mixture is extracted with chloroform. The extracts are combined and concentrated to dryness. The residue is dissolved in 8% (W/V) alcoholic ammonia (50 ml) and the solution is allowed to stand at room temperature to give the above-identified compound (8.9 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04571423 |
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| Source dataset | uspto-grants-1986_02 |
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| ORD ID | ord-1378c903e2834285ad1631d1f6cadfcc |
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| Source note | uspto-grants-1986_02 |
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