HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 70556883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 70559453 | HCID 70559453 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70556883 | HCID 70556883 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of [[1-(2-benzo[b]thiophen-3-yl-acetyl)-2-benzyloxymethyl-azetidine-2-carbonyl]-(4-chloro-benzyl)-amino]-acetic acid ethyl ester, Intermediate 163 (1 eq.) in DCM at 0° C. was added BBr3. The reaction was stirred at 0° C. for 2 h. The crude was diluted with DCM and poured into a saturated aqueous solution of NaHCO3. The layers were separated, the organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 100/0 to 95/5) to afford [[1-(2-benzo[b]thiophen-3-yl-acetyl)-2-hydroxymethyl-azetidine-2-carbonyl]-(4-chloro-benzyl)-amino]-acetic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759334B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-9eb01d6c708242008a3508c585e5d582 |
| Source note | uspto-grants-2014_06 |