Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748299Generated: October 30, 2026

Triphenylphosphine → HCID 68323590, compound

https://huagongshe.com/reaction/1748299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantDiethyl 1H-indole-2,6-dicarboxylateHCID 44754779—
ReactantHCID 68323591HCID 68323591—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68323590HCID 68323590—

Reaction Steps

To a solution of tert-butyl {[1-(hydroxymethyl)cyclobutyl]methyl}carbamate (12 g, 55.76 mmol), diethyl 1H-indole-2,6-dicarboxylate (14.56 g, 55.76 mmol) and triphenylphosphine (29.2 g, 111.5 mmol.) in THF (110 mL) is added diisopropyl azodicarboxylate (22.41 mL, 111.5 mmol) at room temperature and the reaction mixture is stirred for 60 h. The solvent is evaporated and the residue is purified by flash column chromatography using 12% EtOAc in petroleum ether to afford diethyl 1-[(1-{[(tert-butoxycarbonyl)amino]methyl}cyclobutyl)methyl]-1H-indole-2,6-dicarboxylate contaminated with un-reacted diethyl 1H-indole-2,6-dicarboxylate. The mixture is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-69731bac2b28448cbc9ecb7c74e67e6d
Source noteuspto-grants-2015_10