HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → HCID 131719746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 70061973 | HCID 70061973 | — |
| Reactant | HCID 70069984 | HCID 70069984 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131719746 | HCID 131719746 | 92% |
Reaction Steps
To a solution of (S,Z)-2-[4-[[[1-[(1,1-dimethylethoxy)carbonyl]-2-pyrrolidinyl]methyl]thio]-2-butenyl]-1H-isoindole-1,3(2H) -dione, (prepared as in Example I, Part A, except substituting 4-bromo-2-butenyl phthalimide for the corresponding phthalimide) (3.60 mmol)) in 2 mL of CH2Cl2 was added 18 mL of 4N HCl/dioxane at 0° C. The ice bath was removed and the reaction was stirred at room temperature for 3 hrs. The reaction mixture was concentrated in vacuo to give title compound (92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05583146 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-9b72998ba6084302a183dfa460b85a69 |
| Source note | uspto-grants-1996_12 |