HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 178519734, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-(Benzyloxy)-6-oxo-1,6-dihydropyridine-2-carboxylic acid | HCID 15450555 | — |
| Reactant | HCID 178527880 | HCID 178527880 | — |
| Product | HCID 178519734 | HCID 178519734 | 83.7% |
Reaction Steps
To a solution of 1-benzyloxy-6-carboxy-2 (1H)-pyridinone (4.90 g, 20 mmol), 2-mercaptothiazoline (2.62 g, 22 mmol), and a catalytic amount of 4-dimethyl-aminopyridine (DMAP) in dry THF (50 mL), was added N,N′-dicyclohexylcarbodiimide (DCC) (4.6 g, 22 mmol). After stirring overnight, the dicyclohexylurea (DCU) solids are removed by filtration the yellow filtrate is removed by rotary evaporation to give a yellow solid. Crystallization from isopropanol-methylene chloride gives the title compound (5.80 g, 83.7%) as a pale yellow powder, m.p.: 135-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557601B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-37b0709f14574092ad760bcf8171185e |
| Source note | uspto-grants-2013_10 |