HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928417Generated: November 1, 2026
Cesium carbonate → {4,6-Dimethyl-5-[({1-[4-(5-methyl-pyrazol-1-ylmethyl)-benzyl]-1H-[1,2,3]triazole-4-carbonyl}-amino)-methyl]-pyridin-2-yl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/928417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | [5-({[1-(4-Chloromethyl-benzyl)-1H-[1,2,3]triazole-4-carbonyl]-amino}-methyl)-4,6-dimethyl-pyridin-2-yl]-carbamic acid tert-butyl ester | HCID 58081302 | — |
| Reactant | HCID 178428694 | HCID 178428694 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {4,6-Dimethyl-5-[({1-[4-(5-methyl-pyrazol-1-ylmethyl)-benzyl]-1H-[1,2,3]triazole-4-carbonyl}-amino)-methyl]-pyridin-2-yl}-carbamic acid tert-butyl ester | HCID 58081322 | — |
Reaction Steps
A mixture of [5-({[1-(4-Chloromethyl-benzyl)-1H-[1,2,3]triazole-4-carbonyl]-amino}-methyl)-4,6-dimethyl-pyridin-2-yl]-carbamic acid tert-butyl ester (200 mg, 0.412 mmol), 3-methylpyrazole (33.9 mg, 0.412 mmol) and cesium carbonate (269 mg, 0.825 mmol) in 2 mL of DMF was stirred at 80° C. for 2 h. The reaction mixture was filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC (Waters SunFire Prep C18 OBD 5 μm 30×100 mm, Flow 40 mL/min, ACN/water (0.1% TFA) 5/95 over 2 min, then ACN/water (0.1% TFA) 5195-100/0 over 15 min). LCMS (Method A) RtA=1.527; [M+H]+=531.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290485B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-37d489d3ea7e4bbcaaf2c45cbf3b371c |
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| Source note | uspto-grants-2016_03 |
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