HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → 2,4-Diallylamino-7-bromothieno[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Allylamino-7-bromo-2-chlorothieno[3,2-d]pyrimidine | HCID 18326469 | — |
| Product | 2,4-Diallylamino-7-bromothieno[3,2-d]pyrimidine | HCID 18326420 | 93.5% |
Reaction Steps
305 mg (1.0 mmol) of 4-allylamino-7-bromo-2-chlorothieno[3,2-d]pyrimidine and 914 mg (16.0 mmol) of allylamine were heated in a sealed tube at 160° C. for 16 hours. After completion of the reaction, the reaction mixture was allowed to resume room temperature, followed by adding a saturated aqueous sodium hydrogen carbonate solution thereto and extraction with ethyl acetate (50 ml×2). After the organic layer was washed with brine and dried over anhydrous sodium sulfate, the solvent was distilled off. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/4) to give 304 mg (yield: 93.3%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06339089B2 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-8620769b61f349f98f2a768d30fe6ecb |
| Source note | uspto-grants-2002_01 |