HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-[(5-Phenylthiophen-2-yl)-methylene]-2-methylpropanesulfinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1-(5-Phenylthiophen-2-yl)ethan-1-amine | HCID 3032019 | — |
| Reactant | N-[1-(5-phenylthiophen-2-yl)ethyl]-2-methylpropanesulfinamide | HCID 66706418 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[(5-Phenylthiophen-2-yl)-methylene]-2-methylpropanesulfinamide | HCID 66706412 | 77% |
Reaction Steps
1-(5-Phenyl-thiophen-2-yl)ethylamine (Isomer 2, Preparation 171) Add 4N hydrogen chloride in dioxane (1.112 mL, 4.449 mmol) to a stirred solution of N-[1-(5-phenylthiophen-2-yl)ethyl]-2-methylpropanesulfinamide (Isomer 2) (684 mg, 2.225 mmol) in methanol (10 mL) at room temperature. Stir for 2 h and remove the solvent in vacuo to obtain a solid that was washed with ethyl ether. Dissolve the solid in DCM and wash with saturated aqueous NaHCO3. Dry the organic phase over Na2SO4, filter and concentrate in vacuo to obtain the desired intermediate (347 mg, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580780B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-1009c5029a144b02a0e613eca883c4f1 |
| Source note | uspto-grants-2013_11 |