HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643674Generated: October 30, 2026
1,1'-Carbonyldiimidazole → N'-boc-3-(3-(2-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzohydrazide
https://huagongshe.com/reaction/643674
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | 3-(3-(2-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzoic acid | HCID 59261363 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N'-boc-3-(3-(2-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzohydrazide | HCID 59261376 | — |
Reaction Steps
To a solution of 3-(3-(2-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzoic acid (444 mg, 1.22 mmol) in 15 mL of THF at RT was added CDI (218 mg, 1.34 mmol). The resulting mixture was heated for 1 h at 50° C. The reaction mixture was then cooled to RT and tert-butyl carbazate (177 mg, 1.34 mmol) was added. The reaction mixture was again heated at 50° C. for 24 h. After the reaction mixture was concentrated to dryness, the residue was purified on the ISCO (40 g column, 50-100% EtOAc in Hexanes) to afford the title compound as an off-white amorphous solid. MS (ESI, pos. ion) m/z: 478.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700593B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-3133468e29974676a713f41669bf29ea |
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| Source note | uspto-grants-2010_04 |
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