HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 2-(cyclopentylamino)acetate → N-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 2-(cyclopentylamino)acetate | HCID 13298943 | — |
| Reactant | 2-Acetylthio-3-chlorobenzoic acid | HCID 13420405 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl ester | HCID 13420406 | 100% |
Reaction Steps
2-Acetylthio-3-chlorobenzoic acid (11.5 g, 50 mmol) and N-cyclopentylglycine t-butyl ester (10.0 g, 50 mmol) in methylene chloride (350 ml) were cooled to 0°-5° C., and N,N1 -dicyclohexylcarbodiimide (10.3 g, 50 mmol) in methylene chloride (50 ml) was added. The mixture was stirred overnight. The DCC-urea was filtered and washed with CH2Cl2. The filtrate was then washed 2×125 ml 1N HCl, 2×125 ml saturated NaHCO3, 2×125 ml brine, dried (MgSO4), filtered and concentrated to give 20.6 g of an oil. The crude product was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04347246 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-6a0e11892b014bdcbc21695dc4dabf20 |
| Source note | uspto-grants-1982_08 |