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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922309Generated: November 1, 2026

Triphenylphosphine → HCID 44124835, compound

https://huagongshe.com/reaction/1922309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-PyridinepropanolHCID 17861—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(S)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamideHCID 66857149—
SolventDichloromethaneHCID 6344—
ProductHCID 44124835HCID 4412483546.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of N-[(2S)-5-hydroxy-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (50 mg, 0.196 mmol, Description 3) and 3-pyridinepropanol (0.028 ml, 0.215 mmol) in dichloromethane (1 ml) was added diisopropyl azodicarboxylate (0.038 ml, 0.196 mmol) followed by triphenylphosphine (51.4 mg, 0.196 mmol). The reaction mixture was stirred at 25° C. overnight. Solvent was removed under vacuum and the crude product was purified by reverse phase chromatography using the MDAP. Relevant fractions were combined and concentrated to give 34 mg of material which was dried in the vacuum oven overnight. This solid was then dissolved in DCM (10 ml) and washed with water (2*10 ml). The organic phase was dried over MgSO4 and concentrated. This product was purified by MDAP a second time. This material was dissolved in MeOH and loaded on to a SCX cartridge, washed with MeOH and eluted with methanolic ammonia. Relevant fractions were combined and concentrated to give the title compound as a white solid (2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173820B2
Source datasetuspto-grants-2012_05
ORD IDord-7dd1e592eec34a0381d2b452c4b83484
Source noteuspto-grants-2012_05