HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromotrichloromethane → HCID 67348230, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromotrichloromethane | HCID 6383 | — |
| Reactant | Diazabicyclo[5.4.0]undec-7-ene | HCID 9834010 | — |
| Reactant | HCID 67350582 | HCID 67350582 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67348230 | HCID 67348230 | 87% |
Reaction Steps
Methyl (S)-2-{3-[(S)-9-methylthio-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl]phenyl}-4,5-dihydro-1,3-oxazole-4-carboxylate (138 mg, 0.304 mmol) obtained in Step 1 was dissolved in dichloromethane (5 mL), and the mixture was stirred at room temperature for 2 hours after adding bromotrichloromethane (0.181 mL, 0.913 mmol) and diazabicyclo[5,4,0]undec-7-ene (0.137 mL, 0.913 mmol). The mixture was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give methyl (S)-2-[3-(9-methylthio-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl)phenyl]-1,3-oxazole-4-carboxylate (119 mg, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998954B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-591c280f819b4fdca4bd71fa18dc709d |
| Source note | uspto-grants-2011_08 |