Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21224255 | HCID 21224255 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 21224234 | HCID 21224234 | — |
Reaction Steps
The product from Example 20A, N-tert-butoxy-2-[4-(4-phenoxyphenylsulfonyl)-1-(ethoxycarbonylmethyl)piperidin-4-yl]-acetamide, was dissolved in dichloroethane (10 ml), cooled to 0° C., and saturated with hydrochloric acid gas. The reaction vessel was then sealed and the solution stirred for two days at 25° C. Solvent was removed from the reaction mixture under reduced pressure, and the residue purified by preparative TLC, eluting with 10% methanol/methylene chloride, to give N-hydroxy-2-[4-(4-phenoxyphenylsulfonyl)-1-(ethoxycarbonylmethyl)piperidin-4-yl]-acetamide (420 mg), m/e=477.1 (MH+, FABMS).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932595 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-85c4759cccad4db98a4a93c69b636b83 |
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| Source note | uspto-grants-1999_08 |
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