Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57018702 | HCID 57018702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 69646569 | HCID 69646569 | — |
Reaction Steps
A 4N hydrochloric acid solution in dioxane (2 ml) is added at 0° C. to (2S,4S,5S,7S)-N-[4-(tert-butoxycarbonyl)amino-7-butylcarbamoyl-5-hydroxy-2-isopropyl-8-methyl-nonyl]-2-(3-methoxypropoxy)-benzamide (50 mg). The reaction mixture is stirred at 0° C. for 2 hours (TLC monitoring) and then the solvent is immediately concentrated under a high vacuum with vigorous stirring until frozen and is subsequently removed by lyophilisation. After drying under a high vacuum, (2S,4S,5S,7S)-N-(4-amino-7-butylcarbamoyl-5-hydroxy-2-isopropyl-8-methyl-nonyl)-2-(3-methoxypropoxy)-benzamide hydrochloride is obtained in the form of a foamy solid: Rf (W)=0.31. HPLC Rt =12.8 min. MS(FAB) m/e 522 (M+ +1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05641778 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-5b575b4c717a4dbdb3e65a5ef522b1c5 |
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| Source note | uspto-grants-1997_06 |
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