Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 20134111 | HCID 20134111 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14207946 | HCID 14207946 | 48.4% |
Reaction Steps
To a suspension of 4.00 g of thieno[3,4-b]pyridin-4(1H)-one 9 in 120 ml of acetic acid is added 3.00 g of nitric acid (d=1.38). The reaction mixture is stirred at 70° C. for 3 minutes and cooled to room temperature. The resulting crystals are collected by filtration, and then washed with water and methanol-ether, affording 2.51 g (48%) of Compound 10. An analytical sample is recrystallized from dimethylsulfoxide-methanol to give yellow crystals melting at 329°-332° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753951 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-96540de75fd34db589943b52790753a8 |
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| Source note | uspto-grants-1988_06 |
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