HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86693977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-acetoxyethyl p-nitrophenyl carbonate | HCID 11780560 | — |
| Reactant | (2S,5R)-7-oxo-N-[(3S)-pyrrolidin-3-yloxy]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide | HCID 71714408 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86693977 | HCID 86693977 | — |
Reaction Steps
To a mixture of (2S,5R)-7-oxo-N-[(3S)-pyrrolidin-3-yloxy]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide Compound 2 (Table 1) (0.030 g, 0.086 mmol, Example 2) in DMF (dimethyl formamide) (1.5 mL) was added 1-{[(4-nitrophenoxy)carbonyl]oxy}ethyl acetate 103 (0.027 g, 0.102 mmol, J. Med. Chem., 1988, vol 31, 2, p318-322) and triethylamine (0.023 mL. 0.171 mmol) sequentially at room temperature. The mixture was stirred at room temperature overnight, diluted with DCM and concentrated to provide a residue, which was subjected to chromatography and preparative HPLC to give Compound 101 (Table 1) (0.011 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796257B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-470c42bffff84566b55425085ef7db01 |
| Source note | uspto-grants-2014_08 |