HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705305Generated: October 25, 2026
Methane → tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-(thiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamate
https://huagongshe.com/reaction/705305
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Ethynylthiophene | HCID 3548422 | — |
| Reactant | tert-butyl (3R,4S,5S)-4-azido-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamate | HCID 86705273 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-(thiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamate | HCID 86705272 | 48% |
Reaction Steps
In a high pressure vial was added tert-butyl (3R,4S,5S)-4-azido-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamate (1.0 equiv.), copper in charcoal (0.4 equiv.), 3-ethynyl thiophene (5.0 equiv.) and triethylamine (1.0 equiv.), in dioxane (0.09 M) to give a black suspension. The pressure tube was sealed and the mixture was stirred with heating to 100° C. overnight. The reaction was cooled to RT, filtered through celite, concentrated to yield tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-(thiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamate in 48% yield. LC/MS (m/z)=691.2 (MH+), Rt=0.98 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173883B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3916b7f6946f4fe1920ac535d8fd7155 |
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| Source note | uspto-grants-2015_11 |
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