HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-hydrazinopyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Chloro-pyrimidine-5-carboxylic acid ethyl ester | HCID 10487815 | — |
| Reactant | 2-Chloropyrimidine-5-carbonyl chloride | HCID 10631129 | — |
| Product | Ethyl 4-hydrazinopyrimidine-5-carboxylate | HCID 21220648 | 44% |
Reaction Steps
The title compound was prepared by (a) treating 2-chloropyrimidine-5-carbonylchloride (Example 13, 110 mg, 0.62 mmol) with ethanol (200 mg, 4.4 mmol in 1 mL of ethyl acetate) to provide 60% of ethyl 2-chloropyrimidine-5-carboxylate, (b) reaction of ethyl 2-chloropyrimidine-5-carboxylate (70 mg, 0.37 mmol) with hydrazine (100 mg, 3 mmol) to afford 44% of ethyl 4-hydrazinopyrimidine-5-carboxylate as in Example 19, (c) reaction of ethyl 4-hydrazinopyrimidine-5-carboxylate (0.36 g, 2.0 mmol) with citraconic anhydride (0.34 g, 3.0 mmol) in analogy to Example 21 to afford 10% (0.05 g) of the title compound; m.p. 95-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935966 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-b1337df3f0094a7baeece8cfaeee93a2 |
| Source note | uspto-grants-1999_08 |