Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Methoxy-2-naphthoic acid | HCID 70161 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178486594 | HCID 178486594 | — |
Reaction Steps
To a mixture of 8.2 g. of 3-methoxy-2-naphthoic acid, 5.2 g. of aminotetrazole, and 80 ml. of pyridine was added dropwise 6.4 ml. of thionyl chloride, maintaining the temperature below 70° C. After stirring for one hour, the mixture was cooled to 25° C. and evaporated to dryness. The residue was washed with dilute hydrochloric acid, then recrystallized from N,N-dimethylformamide, then dissolved in base, filtered, reprecipitated with dilute acid, filtered, washed with methanol, then recrystallized again from N,N-dimethylformamide to provide 3-methoxy-N-(tetrazol-5-yl)naphthalene-2-carboxamide (a type IV compound), m.p. 280°-283° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04432986 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-cdc1de1a1b6f4cafadf85ba5fafa7550 |
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| Source note | uspto-grants-1984_02 |
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