HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 118071484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 72948196 | HCID 72948196 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118071484 | HCID 118071484 | 98.3% |
Reaction Steps
To a mixture of 3-{2-[(difluoroacetyl)amino]ethyl}-5-methoxy-N-methyl-1H-indole-2-carboxamide (2.52 g) and dichloromethane (50.0 mL) was added boron tribromide (1.0 M dichloromethane solution, 23.3 mL) under ice-cooling, followed by slowly warming to room temperature, and then stirring at room temperature overnight. The reaction mixture was cooled to −15° C. and methanol (5.00 mL) was added thereto, followed by warming to room temperature. The reaction mixture was concentrated under reduced pressure and then the residue was purified by silica gel column chromatography (chloroform:methanol=100:0 to 5:1) to obtain 3-{2-[(difluoroacetyl)amino]ethyl}-5-hydroxy-N-methyl-1H-indole-2-carboxamide (2.37 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260445B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-0a6d9e7e2d8d4bd4a62d1275a30265b4 |
| Source note | uspto-grants-2016_02 |