HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → 1-Ethoxycarbonyl-4-((benzothiazol-2-yl)methyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Benzyl-4-((benzothiazol-2-yl)methyl)piperidine | HCID 21180710 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Ethoxycarbonyl-4-((benzothiazol-2-yl)methyl)piperidine | HCID 21180779 | 67.8% |
Reaction Steps
A solution of 500 mg of 1-benzyl-4-((benzothiazol-2-yl)methyl)piperidine (from EXAMPLE 163, Step D) in 10 mL of THF was added 185 mg of ethyl chloroformate at rt. The reaction was stirred at rt for 5 h. The reaction mixture was partitioned between H2O and EtOAc. The aqueous phase was extracted with EtOAc (3×). The combined organic phases were washed with sat'd NaCl and dried over MgSO4. Concentration afforded 320 mg of the title compound as a oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265434B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-d1675590bc0d469b85cf20ad9de1a05f |
| Source note | uspto-grants-2001_07 |