Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57753077 | HCID 57753077 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69076461 | HCID 69076461 | — |
Reaction Steps
A mixture of 9.52 g of 4-chloro-2-(4-chloro-2,5-difluorophenyl)thieno[3,2-d]pyrimidine, 3.13 g of hexamethyleneimine, 10.50 ml of diisopropyl ethylamine and 190 ml of acetonitrile was stirred for 5 hours at 70° C. 600 ml of water was added to the reaction mixture and the precipitate was filtered, washed with water and dried at 50° C. under reduced pressure. The obtained solid was dissolved in 40 ml of THF. The solution was added to 15 ml of 4M HCl-EtOAc solution and concentrated under reduced pressure to give a solid. Through recrystallization of this solid from EtOH-ether, 10.97 g of 4-azepane-1-yl-2-(4-chloro-2,5-difluorophenyl)thieno[3,2-d]pyrimidine hydrochloride was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557112B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-e745b5af03e84bda991a2deb5f7833d6 |
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| Source note | uspto-grants-2009_07 |
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