Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 53967990 | HCID 53967990 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57480416 | HCID 57480416 | — |
Reaction Steps
30 mg of 5(S)-(tert-butoxycarbonyl) amino-4(S)-hydroxy-2(S)-isopropyl-7(S)-[4-(3-hydroxypropoxy)-3-(3-methoxypropoxy)-benzyl]-8-methyl-nonanoic acid N-(2-morpholin-4-yl-ethyl)amide are dissolved in 1.5 ml of a 4N solution, cooled to 0° C., of hydrochloric acid in dioxane and the solution is stirred further for 10 minutes at 0° C. The reaction mixture is concentrated to dryness by evaporation under reduced pressure at room temperature. The residue is purified by means of FC (5 g of silica gel, dichloromethane/methanol 98:2) to yield the title compound: Rf (dichloromethane/methanol 8:2)=0.20; Rt =10.43 minutes; FAB-MS (M+H)+ =610.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606078 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-147c3ad568c645e7b29a186b6bb135ee |
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| Source note | uspto-grants-1997_02 |
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