HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875085Generated: November 2, 2026
2-azido-N-({4-bromo-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-4-chloro-1H-imidazole-5-carboxamide → HCID 178509908, compound
https://huagongshe.com/reaction/1875085
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-azido-N-({4-bromo-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-4-chloro-1H-imidazole-5-carboxamide | HCID 178509910 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178509908 | HCID 178509908 | 44.7% |
Reaction Steps
Lindlar Catalyst (0.167 g, 0.078 mmol) was added to a suspension of 2-azido-N-({4-bromo-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-4-chloro-1H-imidazole-5-carboxamide (0.824 g, 1.569 mmol) in ethyl acetate (30 mL) in a pressure vessel. The vessel was evacuated and flushed with nitrogen, then evacuated and filled with hydrogen (50 psi). The reaction mixture was stirred for 7 h, then filtered through celite. The filtrate was evaporated to dryness and the residue was triturated with ethanol and dried under vacuum to give the title compound (0.350 g, 44%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.95 (br. s., 1H), 7.80 (s, 1H), 7.76 (t, 1H), 7.60 (d, 1H), 7.48 (s, 1H), 7.42 (m, 1H), 7.26 (t, 1H), 5.79 (br. s., 2H), 4.45 (d, 2H). ES MS m/z 498 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-39c2f1a1736b473b8006d54d6f847cc6 |
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| Source note | uspto-grants-2012_11 |
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