HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 6-amino-1,5-dihydro-1-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)-4H-imidazo[4,5-c]pyridine-4-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 54238159 | HCID 54238159 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-amino-1,5-dihydro-1-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)-4H-imidazo[4,5-c]pyridine-4-thione | HCID 22819082 | — |
Reaction Steps
A mixture of 8 g of 4-cyano-5-cyanomethyl-1-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)imidazole, 250 ml of ethanol saturated at 0° C. with hydrogen sulfide, and 2.5 g of triethylamine is kept in a steel bomb for 48 hours at ambient temperature. The reaction solution is evaporated in vacuo to a yellow foam which is coevaporated with ethanol several times to provide 6-amino-1,5-dihydro-1-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-4H-imidazo[4,5-c]pyridine-4-thione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04315000 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-44fc597d4e9e4a3d8c9d383edd0eeb3a |
| Source note | uspto-grants-1982_02 |