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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408612Generated: October 30, 2026

Boron tribromide → HCID 70556883, compound

https://huagongshe.com/reaction/408612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 70559453HCID 70559453—
SolventDichloromethaneHCID 6344—
ProductHCID 70556883HCID 70556883—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-9eb01d6c708242008a3508c585e5d582
Source noteuspto-grants-2014_06