HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → HCID 23368448, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86750032 | HCID 86750032 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23368448 | HCID 23368448 | — |
Reaction Steps
To a suspension of 0.45 g of 3-(2-tert-butoxycarbonylamino-3-hydroxypropoxy)-5-formylamino-1,2-benzoisoxazole in 9 ml of methylene chloride are added 0.14 g of 3,4-dihydro-2H-pyran and 0.06 g of pyridinium p-toluenesulfonate at 20°-25° C., and they are subjected to reaction at 40° C. for one hour. Water is added to the reaction mixture and the pH is adjusted to 9 with a saturated aqueous sodium hydrogencarbonate solution, after which the organic layer is separated. The separated organic layer is dried over anhydrous magnesium sulfate, and the solvent is then removed by distillation under reduced pressure, to obtain oily 3-[2-tert-butoxycarbonylamino-3-(2,3,4,5-tetrahydropyranyloxy)propoxy]-5-formylamino-1,2-benzoisoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578627 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-73b05ea0ece94785a9e23f8e33ce9e71 |
| Source note | uspto-grants-1996_11 |