HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl [(S)-1-(1-cyanocyclopropylcarbamoyl)-3,3-difluorobutyl]carbamate → N-(1-cyanocyclopropyl)-(S)-2-amino-4,4-difluoropentanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl [(S)-1-(1-cyanocyclopropylcarbamoyl)-3,3-difluorobutyl]carbamate | HCID 68974749 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | N-(1-cyanocyclopropyl)-(S)-2-amino-4,4-difluoropentanamide | HCID 66661333 | — |
Reaction Steps
To detach the Boc protecting group, the compound from example 17 (580 mg, 1.83 mmol) was admixed with 10 ml of 1:1 TFA/DCM and stirred at RT for 30 min. Subsequently, the mixture was concentrated by evaporation under reduced pressure and subjected to azeotropic distillation with dichloromethane and toluene, and solvent residues were removed under high vacuum. The product was present as the trifluoroaceate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039480B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-1eac99ec42b745c580f1c49079bac958 |
| Source note | uspto-grants-2011_10 |