Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 5-Amino-3-(3-chloro-phenylamino)-4-cyano-pyrazole | HCID 10681167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178478160 | HCID 178478160 | — |
Reaction Steps
A mixture of 1 g (4.28 mmol) of 5-amino-3-(3-chloro-phenylamino)-4-cyano-pyrazole (Step 49.1), 3.67 g (34.25 mmol) of benzylamine, 0.245 ml (4.28 mmol) of glacial acetic acid and 0.73 ml (19.35 mmol) of formic acid is heated at 200° C. for 20 hours. The reaction mixture is cooled to RT, 30 ml of ice-water and 5 ml of ethanol are added and stirring is carried out for a further 20 minutes. The reaction mixture is then filtered and the filter residue is washed with water. Recrystallization from isopropyl alcohol yields the title compound; m.p. 215-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981533 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-fa79d5a82f7a403eb5e17f93179d91dd |
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| Source note | uspto-grants-1999_11 |
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