HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butyl nitrite → 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Antimony trichloride | HCID 24814 | — |
| Reactant | 4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amine | HCID 5324413 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine | HCID 14116871 | 43% |
Reaction Steps
To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (500 mg, 2.97 mmol) in 1,2-dichloroethane (40 mL) at −10° C. under argon was added antimony chloride (750 mg, 3.29 mmol). After stirring for 5 min, tert-butylnitrite (2.50 mL, 20.8 mmol) was added to the solution. The reaction was stirred at −10° C. for 3 h. The reaction was diluted with CHCl3 (100 mL) and poured into ice water (50 mL). The CHCl3 layer was separated, washed with brine (20 mL), dried with Na2SO4, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 239 mg (43%) of 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354532B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-043e88357cbb4916b8a6324b66b8f7c5 |
| Source note | uspto-grants-2013_01 |