HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 135984695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 135984699 | HCID 135984699 | — |
| Reactant | HCID 135984706 | HCID 135984706 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 135984695 | HCID 135984695 | — |
Reaction Steps
To a mixture of 4-pentyl-8-pyrimidin-4-yl-1,4-dihydro-5H-[1,2,4]triazolo[5,1-i]purin-5-one (14C1) and 6-pentyl-3-pyrimidin-4-yl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one (14C2) (25 mg, 0.15 mmol) in THF (5 mL) was added N-bromosuccinimide (19 mg, 0.22 mmol). The reaction mixture was stirred at room temperature for 1 hour, then the reaction was quenched by phenol. After removing the solvent, the residue was purified using preparative LCMS (method B) to yield the pure compound (14D1) and the pure compound 14D2 respectively. LCMS calculated for C15H16BrN8O (M+H): 403.1; found: 403.0, 405.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462624B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-215d599cff5a452f9c9872bc73de41e3 |
| Source note | uspto-grants-2008_12 |