HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 2-(1-methyl-3-(N-methyl-N-(4-octylphenyl)sulfamoylamino)piperidin-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloroethyl chlorosulfonylcarbamate | HCID 13118812 | — |
| Reactant | N-methyl-4-octylaniline | HCID 17827013 | — |
| Reactant | Methyl 2-(3-amino-1-methylpiperidin-3-yl)acetate | HCID 66864584 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(1-methyl-3-(N-methyl-N-(4-octylphenyl)sulfamoylamino)piperidin-3-yl)acetate | HCID 66864939 | 22% |
Reaction Steps
To a solution of methyl 2-(3-amino-1-methylpiperidin-3-yl)acetate (186 mg, 1 mmol) and Et3N (0.42 mL, 3 mmol) in CH2Cl2 was added the solution of 2-chloroethyl chlorosulfonylcarbamate in CH2Cl2 (0.77 M, 1.3 mL, 1 mmol). After addition, the resulting mixture was stirred overnight at rt. Evaporation of solvents gave a light yellow oil which was used without further purification. A solution of this crude mixture, N-methyl-4-octylaniline (241 mg, 1.1 mmol) and Et3N (0.42 mL, 3 mmol) in CH3CN (10 mL) was refluxed for 2 h. After cooling to rt and evaporating solvents, the residue was purified by a short column (EtOAc/hexance=10:1) to give the title compound (105 mg, 22%) as white solid. MS ESI 468.3 [M+H]+, calcd for [C24H41N3O4S+H]+ 468.29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680282B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-db0448d255ff46a59408ab78dcf93b73 |
| Source note | uspto-grants-2014_03 |