HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448234Generated: October 30, 2026
Lithium Hexamethyldisilazide → tert-Butyl {(3S,5S)-5-(2,3-difluorophenyl)-2-oxo-1-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]piperidin-3-yl}carbamate
https://huagongshe.com/reaction/448234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (2S)-2-(Trifluoromethyl)oxirane | HCID 7171781 | — |
| Reactant | tert-butyl[(3S,5S)-5-(2,3-difluorophenyl)-2-oxopiperidin-3-yl]carbamate | HCID 69096669 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tetrahydrofuran N-methylpyrrolidinone | HCID 22156051 | — |
| Product | tert-Butyl {(3S,5S)-5-(2,3-difluorophenyl)-2-oxo-1-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]piperidin-3-yl}carbamate | HCID 86665203 | — |
Reaction Steps
To a pre-cooled −30° C. solution of tert-butyl[(3S,5S)-5-(2,3-difluorophenyl)-2-oxopiperidin-3-yl]carbamate (described in Intermediate 11, step B, 56 mg, 0.172 mmol) in tetrahydrofuran:N-methyl-2-pyrrolidinone (2:1, 0.8 mL) was added lithium bis(trimethylsilyl)amide (0.22 mL, 0.22 mmol, 1 M in THF) and the mixture was stirred at −30° C. for 30 min. (2S)-2-(Trifluoromethyl)oxirane (19 mg, 0.172 mmol) was added and the resulting mixture was stirred at −30° C. for 2 h. The mixture was diluted with water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water, brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (0% ethyl acetate→90% ethyl acetate/hexane) afforded the title compound. MS: m/z=461.2 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481556B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-9c09d843f6e3479182a07bb2d890fac2 |
|---|
| Source note | uspto-grants-2013_07 |
|---|