HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(Piperidin-1-yl)pyrazine-2-carboxylic acid → HCID 178522719, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(Piperidin-1-yl)pyrazine-2-carboxylic acid | HCID 1282540 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Pivaloyl chloride | HCID 62493 | — |
| Product | HCID 178522719 | HCID 178522719 | — |
Reaction Steps
To a suspension fo 1.28 g of 6-(1-piperidinyl) pyrazine-2-carboxylic acid in 18 ml of tetrahydrofuran, 0.95 ml of triethylamine and 0.84 ml of pivaloyl chloride were added dropwise successively at 0 ° C. under stirring. After stirring for 1 hour at 0 ° C., 0.58 g of 5-amino-1H-tetrazole was added to the mixture, and the reaction mixture was stirred for 30 minutes at room temperature, and then refluxed for 12 hours. The reaction mixture was evaporated, and water was added to the residue. The precipitate was collected by filtration, and recrystalized from a mixture of dimethylsulfoxide and methanol affording 0.55 g of the desired compound as yellow columns. The obtained crystal was consistent with that of (a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792547 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-ae69f077e70c41669af0d3b2dac91c0e |
| Source note | uspto-grants-1988_12 |