HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 178515098, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-chloro-6-fluoro-7-methoxy-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one | HCID 57722844 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178515098 | HCID 178515098 | — |
Reaction Steps
To a stirred solution of 3-chloro-6-fluoro-7-methoxy-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (2.0 g, 6.9 mmol) in CH2Cl2 (100 mL) was added BBr3 (1 M in CH2Cl2, 27.6 mL, 27.6 mmol) at −78° C. The mixture was allowed to warm to room temperature as the bath did. After 6 h at room temperature, the mixture was cooled to 0° C. and treated with aqueous NaHCO3 solution. The yellow precipitate was filtered, washed with CH2Cl2, and dried under high-vacuum overnight to afford the title compound. 1H NMR (600 MHz, CD3SOCD3) δ 8.93 (d, 1H); 8.28 (d, 1H); 7.46 (d, 1H); 7.37 (d, 1H); 7.33 (t, 1H); 7.08 (d, 1H). LRMS (ESI) calc'd for (C14H7ClFNO2) [M+H]+, 276.0; found 276.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207186B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-b32ec742280d45288b2bfa6adaf9547f |
| Source note | uspto-grants-2012_06 |