HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 18801449, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sec-Butylamine | HCID 24874 | — |
| Reactant | 2,4-Dichloro-6-methyl-5-nitropyrimidine | HCID 275294 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18801449 | HCID 18801449 | 57.2% |
Reaction Steps
15 ml of triethylamine are added to a solution of 15.6 g of 2,4-dichloro-5-nitro-6-methylpyrimidine (0.075 mole) in 300 ml of absolute ethanol. With ice cooling, 6.6 g of sec. butylamine (0.09 mole) are added dropwise at 0°-5° C over the course of c. 40 minutes to the dark red solution. After the mixture has been stirred for c. 3/4 hour at this temperature, it is poured into c. 700 ml of ice water and the water is extracted 3 times with ether. The ethereal extracts are dried over magnesium sulphate and evaporated. The resultant red oily substance is crystallised from petroleum ether to yield 10.5 g of 2-chloro-4-sec. butylamino-5-nitro-6-methyl-pyrimidine of m.p. 40°-43° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014677 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-0a1bf8bb37514a25a31e722ca7ff5bd9 |
| Source note | uspto-grants-1977_03 |