HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 15675830, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 15675820 | HCID 15675820 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15675830 | HCID 15675830 | 80% |
Reaction Steps
N-bromosuccinimide was added at room temperature to a solution of 1.675 g (6 mmoles) of 3-bromo-8-ethyl-5-methyl-8H-pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidine (prepared as described in Example 13) dissolved in 12 ml of chloroform, and the mixture was stirred for 2 hours. At the end of this time, the reaction mixture was washed with a 2N aqueous solution of potassium hydroxide and then with water, after which it was dried over anhydrous sodium sulfate and then concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel (eluted with chloroform) and recrystallized from ethyl acetate to afford 1.72 g (yield 80%) of the title compound as colorless needles, melting at 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055479 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-6260ea440c7a462db3db89268b0cb31c |
| Source note | uspto-grants-1991_10 |