HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-tert-butyl hydrogen (2RS,4SR,5SR)-1-{2-[3-(3-methylphenyl)ureido]acetyl}-5-phenylpyrrolidine-2,4-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-tert-butyl 4-methyl (2RS,4RS,5SR)-1-{2-[3-(3-methylphenyl)ureido]acetyl}-5-phenylpyrrolidine-2,4-dicarboxylate | HCID 86751903 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-tert-butyl hydrogen (2RS,4SR,5SR)-1-{2-[3-(3-methylphenyl)ureido]acetyl}-5-phenylpyrrolidine-2,4-dicarboxylate | HCID 86751902 | 45% |
Reaction Steps
A The reaction is carried out in a way analogous to that described in Example 3, but from 1.6 g of 2-tert-butyl 4-methyl (2RS,4RS,5SR)-1-{2-[3-(3-methylphenyl)ureido]acetyl}-5-phenylpyrrolidine-2,4-dicarboxylate and 0.18 g of potassium hydroxide in 20 cm3 of distilled water and 60 cm3 of methanol. After treatment, there is obtained 0.7 g of 2-tert-butyl hydrogen (2RS,4SR,5SR)-1-{2-[3-(3-methylphenyl)ureido]acetyl}-5-phenylpyrrolidine-2,4-dicarboxylate, melting at 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05707991 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-43700cb820e64f84a1214b00afca4401 |
| Source note | uspto-grants-1998_01 |