HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809184Generated: November 1, 2026
Hydrochloric Acid → HCID 178430717, compound
https://huagongshe.com/reaction/1809184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 178430705 | HCID 178430705 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178430717 | HCID 178430717 | 76% |
Reaction Steps
To a solution of KOH (6 g, 154 mmol) in water (46 mL) at 5° C. is added slowly bromine followed by 3-hydroxy-6-methyl-pyrazine-2-carboxylic acid amide (2.6 g, 17.0 mmol) with rapid stirring. The reaction mixture is warmed to 85° C. and stirred for 1 h 30 min. The reaction is cooled to 20° C. and acidified with HCl conc, basified with ammonium hydroxide conc. and left stand overnight at r.t. The solid obtained is filtered and washed with cold water, dried with air and then dried further in a vacuum oven at 60° C. to give 3-amino-5-methyl-pyrazin-2-ol as a beige solid (1.63 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08362018B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-30afc2337d4342ccacc65b92c1b18a04 |
|---|
| Source note | uspto-grants-2013_01 |
|---|