Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 1h-pyrrole-2-carbohydrazide | HCID 281610 | — |
| Reactant | HCID 14086187 | HCID 14086187 | — |
| Reactant | HCID 178527898 | HCID 178527898 | — |
| Product | HCID 178482478 | HCID 178482478 | — |
Reaction Steps
A mixture of 2-(2-pyrrolyl)-5-thiono-5,6-dihydro[1,2,4]triazolo[1,5-c]quinazoline (4.28 g), prepared from 5-chloro-2-isothiocyanatobenzonitrile and 2-pyrrolecarbohydrazide as described in Example 39, is placed in a stainless steel pressure vessel with 40% aqueous methylamine saturated at 0° with methylamine gas (225 ml) and heated 6 hours at an outside temperature of 150° C. The reaction mixture is cooled to room temperature and the solid collected, washed with water and air dried. Recrystallization from aqueous methanol, then water affords pure 5-methylimino-5,6-dihydro-2-(2-pyrrolyl)-[1,2,4]triazolo-[1,5-c]quinazoline, mp 220°-221°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04713383 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-25c8ae493b904616aeccc8b60e5164a4 |
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| Source note | uspto-grants-1987_12 |
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