HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → HCID 131733201, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 131733202 | HCID 131733202 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131733201 | HCID 131733201 | — |
Reaction Steps
To a solution of (2S,4S)-4-(tert-butyl-dimethyl-silanyloxymethyl)-2-(3-chloro-2-fluoro-benzyl carbamoyl)-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester (200 mg, 0.35 mmol) in CH2Cl2 (10 mL) under N2 atmosphere at −78° C. was added DAST (92 μL, 0.7 mmol). The reaction mixture was then allowed to reach RT and further stirred for 1.5 h then poured into an aqueous saturated solution of NaHCO3 and extracted twice with CH2Cl2. The combined organic layers were dried (Na2SO4), filtered and concentrated to give the desired material which was used without further purification in the next step. TLC, Rf (c-hexane/EtOAc 1:1)=0.75; MS (LC/MS): 541.2/543.1 [M+Na]+, 463.1/465.1 [MH−tBu]+, 419.0/421.1 [MH−Boc]+; tR (HPLC conditions f): 2.81 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09085555B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-af0d58b1465b4c3e9eed1922f803da8d |
| Source note | uspto-grants-2015_07 |