HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559698Generated: October 29, 2026
Methyl N-(triethylammoniosulfonyl)carbamate → HCID 66727508, compound
https://huagongshe.com/reaction/559698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl N-(triethylammoniosulfonyl)carbamate | HCID 2724994 | — |
| Reactant | HCID 59278349 | HCID 59278349 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66727508 | HCID 66727508 | — |
Reaction Steps
To a solution of (2S,3R)-2-(2-{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-butyrylamino)-3-hydroxy-butyric acid methyl ester (0.900 g, 1.96 mmol) in THF (20.0 mL) was added Burgess reagent (0.586 g, 2.46 mmol). The mixture was warmed at reflux for 23 hours. The mixture was then concentrated in vacuo, dissolved in ethyl acetate (100 mL) and washed with saturated aqueous sodium bicarbonate (50 mL) and brine (50 mL). The organic layer was dried over MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 0-10% methanol in ethyl acetate to afford (4S,5S)-2-(1-{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-propyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester as white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063065B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-232d3c21a3a949f98d1f0dd314a40f5d |
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| Source note | uspto-grants-2011_11 |
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