HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → N,N-diethyl-1-methyl-[1,2,4]triazolo[4,3-a]quinoxalin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | 4-Chloro[1,2,4]triazolo[4,3-a]quinoxaline | HCID 1126118 | — |
| Reactant | 4-Chloro-1-methyl[1,2,4]triazolo[4,3-a]quinoxaline | HCID 2768643 | — |
| Product | N,N-diethyl-1-methyl-[1,2,4]triazolo[4,3-a]quinoxalin-4-amine | HCID 899504 | 54% |
Reaction Steps
This compound was prepared by the method of Example 11, utilizing 4-chloro-1-methyl-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 3) as starting material in place of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) and diethylamine as reagent in place of di-n-propylamine. The crude product obtained was recrystallized from chloroform and then from cyclohexane to afford 7.2 g. (54% yield) of pure 4-diethylamino-1-methyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 123°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623725 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-71cebf7c53bb4a4f94011102eb89c88d |
| Source note | uspto-grants-1986_11 |