Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | ((2-Thienylcarbonyl)amino)acetic acid | HCID 679227 | — |
| Reactant | 2-Methoxypyridine-4-carbaldehyde | HCID 2762996 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 75238444 | HCID 75238444 | 81.5% |
Reaction Steps
A mixture of N-(2-thienylcarbonyl)glycine (454 mg, 2.45 mmol), 2-methoxy-4-pyridinecarboxaldehyde (370 mg, 2.7 mmol), sodium acetate (201 mg, 2.45 mmol) and acetic anhydride (3.0 mL) was stirred at 90° C. for 3 hours in a sealed tube. Thereafter, the temperature of the reaction solution was returned to room temperature, and water (15 mL) was then added thereto. The obtained mixture was stirred at the same temperature as described above for 1 hour. Thereafter, the precipitated crystal was collected by filtration, and it was washed with water (50 mL) and was then dried under reduced pressure, so as to obtain 572 mg of the above-captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018238B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-cee5b1a370bd426dbb47688c10c7598f |
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| Source note | uspto-grants-2015_04 |
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