HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922309Generated: November 1, 2026
Triphenylphosphine → HCID 44124835, compound
https://huagongshe.com/reaction/1922309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Pyridinepropanol | HCID 17861 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (S)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide | HCID 66857149 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44124835 | HCID 44124835 | 46.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173820B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7dd1e592eec34a0381d2b452c4b83484 |
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| Source note | uspto-grants-2012_05 |
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