HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 5-([1,1'-biphenyl]-2-yl)-5-aminopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methyl 5-([1,1'-biphenyl]-2-yl)-5-(1,1-dimethylethylsulfinamido)pentanoate | HCID 69081687 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-([1,1'-biphenyl]-2-yl)-5-aminopentanoate | HCID 69083690 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A cooled (0° C.) slightly yellow solution of methyl 5-([1,1′-biphenyl]-2-yl)-5-(1,1-dimethylethylsulfinamido)pentanoate (270 mg; 0.69 mmol) in MeOH (4 ml) was treated dropwise with a solution of 4 M HCl in 1,4-dioxane (0.35 ml; 1.40 mmol). The resulting yellow mixture was further stirred at 0° C., under nitrogen, for 10 min., and then at rt for 1 h. The reaction mixture was then concentrated to dryness under reduced pressure and the colorless solid residue was further dried under HV to give the chlorhydrate salt of methyl 5-([1,1′-biphenyl]-2-yl)-5-aminopentanoate as a colorless solid. LC-MS (conditions A): tR=0.57 min.; [M+H]+: 284.13 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-0ee16f3b2d534657bb0830ae20c4630a |
| Source note | uspto-grants-2016_01 |