HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 6-amino-6-(3,5-dimethoxypyridin-4-yl)hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methyl 6-(3,5-dimethoxypyridin-4-yl)-6-(1,1-dimethylethylsulfinamido)hexanoate | HCID 69083411 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 6-amino-6-(3,5-dimethoxypyridin-4-yl)hexanoate | HCID 69085562 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A cooled (0° C.) yellow solution of methyl 6-(3,5-dimethoxypyridin-4-yl)-6-(1,1-dimethylethylsulfinamido)hexanoate (506 mg; 1.30 mmol) in MeOH (9 ml) was treated dropwise with a solution of 4 M HCl in 1,4-dioxane (0.65 ml; 2.60 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 yellow oily residue was further dried under HV to give the chlorhydrate salt of methyl 6-amino-6-(3,5-dimethoxypyridin-4-yl)hexanoate as a brown solid. LC-MS (conditions A): tR=0.36 min.; [M+H]+: 284.25 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-9afc0a74f9a24ae684328d59aee31bf1 |
| Source note | uspto-grants-2016_01 |