HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dioxolane → HCID 66970476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dioxolane | HCID 12586 | — |
| Reactant | tert-Butyl 4-fluoro-2-(5-nitro-4-thiocyanatopyrimidin-2-ylamino)phenylcarbamate | HCID 59704889 | — |
| Reactant | HCID 66926982 | HCID 66926982 | — |
| Reactant | HCID 66970493 | HCID 66970493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66970476 | HCID 66970476 | — |
Reaction Steps
1,3-Dioxolane of (R)-tert-butyl 4-fluoro-2-(5-nitro-4-(4-oxo-1,2,3,4-tetrahydronaphthalen-1-ylamino)pyrimidin-2-ylamino)phenylcarbamate. A solution of tert-butyl 4 fluoro-2-(5-nitro-4-thiocyanatopyrimidin-2-ylamino)phenylcarbamate (170 mg), 1,3-Dioxolane of (R)-4-amino-3,4-dihydronaphthalen-1(2H)-one (85 mg), and TEA (0.2 mL) in DMF (5 mL) was stirred at room temperature overnight. The reaction mixture was diluted with EtOAc, washed with saturated brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by PTLC (EtOAc/hexane, 50/50) to afford 150 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884109B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-96314ac450ab4985985ebbdfc7558b18 |
| Source note | uspto-grants-2011_02 |