HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922307Generated: October 31, 2026
Hydrochloric Acid → HCID 131729710, compound
https://huagongshe.com/reaction/1922307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (6-Methylpyridin-3-yl)methanol | HCID 11228788 | — |
| Reactant | (S)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide | HCID 66857149 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131729710 | HCID 131729710 | — |
Reaction Steps
A mixture of N-[(2S)-5-hydroxy-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (700 mg, 2.74 mmol, Description 3) and (6-methyl-3-pyridinyl)methanol (338 mg, 2.74 mmol) in dichloromethane (30 ml) was stirred under argon at room temperature, Triphenylphosphine (719 mg, 2.74 mmol) and diisopropyl azodicarboxylate (0.533 ml, 2.74 mmol) were then successively added. The resulting mixture was stirred at room temperature under argon for 16 hours. The reaction mixture was washed with water, dried over sodium sulphate, filtered and evaporated. The desired product was purified by SCX column eluting with 1 M ammonia in methanol solution and column chromatography on silica using 1 to 99% ethyl acetate in n-pentane to give a white solid. The free base solid was dissolved in methanol and treated with ethereal hydrochloride to give the title compound (554 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-0bf846c3eebf499d8ea2fc7422aec7c2 |
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| Source note | uspto-grants-2012_05 |
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