HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088948Generated: October 30, 2026
Isonicotinic Acid → HCID 178429213, compound
https://huagongshe.com/reaction/1088948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isonicotinic Acid | HCID 5922 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 13589235 | HCID 13589235 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178429213 | HCID 178429213 | — |
Reaction Steps
0.15 ml. Phosphorus oxychloride are added to a solution of 221 mg. (1 mmol) 6-amino-5-nitro-3,3-dimethyl-indolin-2-one in 2 ml. dimethylformamide containing 0.5 ml. pyridine and 123 mg. (4 mmol) isonicotinic acid. The reaction mixture is then stirred for about 3 hours, poured on to ice water and the crystals obtained are filtered off with suction. Subsequently, the product is hydrogenated in 10 ml. ethanol containing 0.2 ml. triethylamine in the presence of Pd/C. The catalyst is then filtered off with suction, the filtrate is evaporated and the residue is heated under reflux for about 6 hours in a solution of 5 ml. ethanol and 1 ml. concentrated hydrochloric acid. The reaction mixture is then evaporated, digested with an aqueous solution of ammonia and the product obtained recrystallised from ethanol/water. Yield: 220 mg. (63% of theory); m.p. 215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04963686 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-3b2c4691d7024ada92e252b95eab3eeb |
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| Source note | uspto-grants-1990_10 |
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