HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Chloro-6-cyano-2-[2-[(diethoxyphosphoryl)acetyl]hydrazino]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Diethoxyphosphoryl)acetyl chloride | HCID 10822542 | — |
| Reactant | 3-Chloro-6-cyano-2-hydrazinoquinoxaline | HCID 19421423 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-6-cyano-2-[2-[(diethoxyphosphoryl)acetyl]hydrazino]quinoxaline | HCID 19421409 | — |
Reaction Steps
A solution of (diethoxyphosphoryl)acetyl chloride (2.15 g, 10 mmol) in 20 ml of dry tetrahydrofuran was added to a solution of 3-chloro-6-cyano-2-hydrazinoquinoxaline (2.0 g, 9 mmol) and dry triethylamine (1.4 ml, 10 mmol) in 100 ml of dry tetrahydrofuran. The mixture was stirred at room temperature overnight, and filtered. The filtrate was evaporated, and the title compound was isolated as a semisolid residue, which was used in the next step without further purification; 1H-NMR (DMSO-d6): δ 1.26 (t, 6H), 3.09 (d, 2H), 4.10 (quint, 4H), 7.71 (d, 1H), 7.97 (dd, 1H), 8.39 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559106 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-b16fc9fb013c473d9bfb47687e8ebbe5 |
| Source note | uspto-grants-1996_09 |