HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283151Generated: October 30, 2026
Cyanoacetamide → 2-Amino-3-quinolinecarboxamide
https://huagongshe.com/reaction/1283151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | 2-Aminobenzaldehyde | HCID 68255 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-3-quinolinecarboxamide | HCID 5200228 | 84% |
Reaction Steps
Cyanoacetamide (19.4 g., 0.23 mole) is added to a solution of sodium ethoxide (6.65 g., 0.29 mole) in absolute ethanol (460 ml.) maintained at 50° C. The mixture is stirred and o-aminobenzaldehyde (28.0 g., 0.23 mole) in absolute ethanol (100 ml.) added. After fifteen minutes stirring at 50° C., the reaction mixture is cooled in an ice bath, filtered and dried to give 34.5 g. (84% yield) of product; m.p. 240°-242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974161 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-4576fa5033ce484287ab4e9e40821703 |
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| Source note | uspto-grants-1976_08 |
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