HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67960573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67960315 | HCID 67960315 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67960573 | HCID 67960573 | — |
Reaction Steps
To 5-((4-methylquinazolin-2-yl)methyl)-7,8-dihydro-3H-imidazo[2,1-b]purin-4(5H)-one 13 (386 mg, 1.16 mmol) in CH3CN (10 ml) was added NBS (268 mg, 1.51 mmol) at 0° C., stirred for 1.5 hr. Another 41 mg of NBS was added, stirred for 30 minutes. The reaction was quenched by adding water (15 ml), washed with DCM (2×15 ml). The organic phase was washed with HCl (1 M, 10 ml). The combined aqueous phase was concentrated and purified by flash chromatography (MeOHIDCM, MeOH contains 1% Et3N) to afford 2-bromo-5-((4-methylquinazolin-2-yl)methyl)-7,8-dihydro-3H-imidazo[2,1-b]purin-4(5H)-one 14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691832B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-160b236dd91d4e95b5db5af6ef0f5538 |
| Source note | uspto-grants-2014_04 |