HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66654727, compound → HCID 66653911, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66654727 | HCID 66654727 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66653911 | HCID 66653911 | — |
Reaction Steps
To an ice-cooled solution of (S)-1-(5-chloro-2-ethoxycarbonylmethoxy-phenyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (790 mg, 1.77 mmol, 1.0 eq.) in DCM (3 mL), 4M HCl in dioxane (7.4 mL) was added. The resulting solution was stirred at r.t. for 1.5 hours. The reaction mixture was concentrated in vacuo. The residue was coevaporated with EtOH (3×). To a solution of the residue in EtOH (2 mL), conc. H2SO4 (0.18 mL) was added. The solution was stirred at r.t. for 18 hours. Water and 5% aq. NaOH soln. were added and the mixture was extracted with Et2O (3×10 mL). The comb. org. phases were dried over MgSO4, filtered, and concentrated in vacuo to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575158B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-44e10bd7bd724c22b9a19e3c2e04f858 |
| Source note | uspto-grants-2013_11 |