HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydride → HCID 20096998, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 2-chloro-N,N-dimethylacetamide | HCID 75886 | — |
| Reactant | HCID 178526302 | HCID 178526302 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20096998 | HCID 20096998 | — |
Reaction Steps
4.6 g (30 mmol) of 7-hydroxy-[1,2,5]oxadiazolo[3,4-d]pyrimidine-1-oxide and 0.28 g (35 mmol) of lithium hydride are heated at 50° C. for 30 minutes in 65 ml of THF. A solution of 4.6 g (38 mmol) of 2-chloro-N,N-dimethylacetamide in 10 ml of THF is then added dropwise and the mixture is heated under reflux for 4 hours. The solvent is completely stripped off in a rotary evaporator and the residue is stirred with 30 ml of water for 2 hours. The precipitate is filtered off with suction and recrystallised from THF, and 2.4 g (33%) of 6-(N,N-dimethylaminocarbonylmethyl)[1,2,5]oxadiazolo[3,4-d]pyrimidine-7(6H)-one-1-oxide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382585 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-56e4d1b1551e488b9cb55439420f886f |
| Source note | uspto-grants-1995_01 |