HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094830Generated: October 26, 2026
Carbon Dioxide → N-[4-Methyl-5-(2-nitrooxy-ethyl)-thiazol-2-yl]-nicotinamide
https://huagongshe.com/reaction/1094830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-[5-(2-hydroxy-ethyl)-4-methyl-thiazol-2-yl]-nicotinamide | HCID 18440895 | — |
| Product | N-[4-Methyl-5-(2-nitrooxy-ethyl)-thiazol-2-yl]-nicotinamide | HCID 18440894 | — |
Reaction Steps
70% nitric acid (1.2 ml) was added to acetic anhydride (5 ml) while stirring and maintaining the temperature between 20-30° C. by external cooling. The mixture was cooled to −5° C. while stirring, followed by the addition of 1 gram of N-[5-(2-hydroxy-ethyl)-4-methyl-thiazol-2-yl]-nicotinamide. After 30 minutes at −5° C. the mixture was heated to 10° C. and stirred for one additional hour. The resulting mixture was poured into ice-water and stirred for 1 hour. Aliquots of NaHCO3 were added until CO2 evolution ceased. The orange-yellow water solution was extracted with three portions of 15 ml ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated by evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08134010B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-9fa71f9740a240909e6e995ddb8f0ff9 |
|---|
| Source note | uspto-grants-2012_03 |
|---|