HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropylamine → HCID 21445068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 4,6-dichloro-2-ethyl-5-nitropyrimidine | HCID 230647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21445068 | HCID 21445068 | 36.3% |
Reaction Steps
28.6 g (0.5 mole) of cyclopropylamine are added dropwise ar -50° C to 55.5 g (0.25 mole) of 2-ethyl-4,6-dichloro-5-nitro-pyrimidine in 1 liter of ethanol. The reaction mixture is stirred for 3 hours at room temperature and then cooled to -40° C. The crystalline precipitate that has formed is filtered off and dried. Yield: 21 g of 2-ethyl-4-chloro-5-nitro-6-cyclopropylamino-pyrimidine of m.p. 61°-62° C. A Further 22 g of 2-ethyl-4-chloro-5-nitro-6-cyclopropylamino-pyrimidine of m.p. 61°-62° C are obtained by evaporating the filtrate, suspending the residue in water, extracting with ether, drying the ethereal extracts over MgSO4 and evaporating them.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014677 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-dfa7d01cbf4645f48ce62164ae632829 |
| Source note | uspto-grants-1977_03 |