HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → di-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | N,N-Diethylethanamine trihydrofluoride | HCID 175505 | — |
| Reactant | di-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-hydroxyethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate | HCID 117812722 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | di-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate | HCID 117812673 | — |
Reaction Steps
Di-tert-butyl (4R)—N-(tert-butoxycarbonyl)-4-{[1-(2-hydroxyethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate (74 mg, 152.7 μmol) was dissolved in tetrahydrofuran (5 ml) and triethyl amine (319 μl, 2.3 mmol), Nonafluorobutanesulfonyl fluoride (185 mg, 611 μmol), and Triethylamine trihydrofluoride (98 mg, 611 mmol) were added subsequently. The mixture was stirred at room temperature for 6 days. The mixture was than concentrated in vacuo, and the residue was purified by silica gel chromatography to yield 30 mg (40%) of slightly impure product, which was used in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238631B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-cd1141b71fa146afa79ebb0b93ce594e |
| Source note | uspto-grants-2016_01 |