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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451317Generated: October 30, 2026

1,2-Dichloroethane → HCID 86699449, compound

https://huagongshe.com/reaction/451317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2-DimethylaminopyridineHCID 21885—
Reactanttert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
Reactant(2S,5R)-6-(Benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acidHCID 57389355—
SolventDichloromethaneHCID 6344—
ProductHCID 86699449HCID 86699449—

Reaction Steps

To a solution of (2S,5R)-6-(phenylmethoxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid (1 g, 3.62 mmol) in dry dichloromethane (30 mL) was added dimethylaminopyridine (884 mgL, 7.24 mmol), EDC (1.388 g, 7.24 mmol), and tert-butyl (3S)-3-aminopyrrolidine-1-carboxylate (742 mg, 3.98 mmol) sequentially at room temperature under nitrogen. The reaction mixture was stirred at room temperature over the weekend. The reaction mixture was then concentrated under vacuum and the residue was purified by HPLC on a 30×100 mm Waters Sunfire column eluted with 15% to 100% CH3CN+0.05% TFA/water+0.05% TFA over 15 minutes to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487093B2
Source datasetuspto-grants-2013_07
ORD IDord-dc90514f15944693baf4c010e81910da
Source noteuspto-grants-2013_07