HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 69543822 | HCID 69543822 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 69543844 | HCID 69543844 | — |
Reaction Steps
(step 5) 2.37 g (4.3 mmol) (2S,4R)-2-[N′-Methyl-N′-(4-methyl-phenylsulfonyl)-hydrazinocarbonyl]-4-(4-methoxy-benzylsulfanyl)-pyrrolidine-1-carboxylic acid 1-tert-butyl ester in 10 ml CH2Cl2 were treated with 4 ml TFA at 0° C. and kept in the freezer over night. The solvent was evaporated, the crude material was dissolved and evaporated with toluene (2×) and hexane (3×) yielding (2S,4R)-2-[N′-Methyl-N′-(4-methyl-phenylsulfonyl)-hydrazinocarbonyl]-4-(4-methoxy-benzylsulfanyl)-pyrrolidine as TFA salt as crude product, which was subjected to the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444829B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-3091c1ba253d40c1bbc2b6be3f172af7 |
| Source note | uspto-grants-2002_09 |