HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875175Generated: October 31, 2026
Sodium Bicarbonate → 4-chloro-N-[(4-chloro-3-{[3-cyano-5-(hydroxymethyl)phenyl]oxy}-2-fluorophenyl)methyl]-2-methyl-1H-imidazole-5-carboxamide
https://huagongshe.com/reaction/1875175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178432877 | HCID 178432877 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-chloro-N-[(4-chloro-3-{[3-cyano-5-(hydroxymethyl)phenyl]oxy}-2-fluorophenyl)methyl]-2-methyl-1H-imidazole-5-carboxamide | HCID 178432878 | 76% |
Reaction Steps
To a solution of 4-chloro-N-({4-chloro-3-[(3-cyano-5-formylphenyl)oxy]-2-fluorophenyl}methyl)-2-methyl-1H-imidazole-5-carboxamide (0.178 g, 0.398 mmol) in methanol (5 ml) at 0° C. was added sodium borohydride (0.015 g, 0.398 mmol) and the reaction mixture was allowed to warm to rt over 30 minutes. The reaction mixture was neutralized with saturated sodium bicarbonate, diluted with EtOAc, and the organic layer was separated. The solvent was evaporated and the crude material was purifed via silica gel chromatography to give 4-chloro-N-[(4-chloro-3-{[3-cyano-5-(hydroxymethyl)phenyl]oxy}-2-fluorophenyl)methyl]-2-methyl-1H-imidazole-5-carboxamide (0.135 g, 0.300 mmol, 76% yield). 1H NMR (400 MHz, METHANOL-d4) δ ppm 7.39 (s, 1H), 7.27-7.38 (m, 2H), 7.18 (s, 1H), 7.08 (s, 1H), 4.60 (s, 2 H), 4.58 (s, 2H), 2.32 (s, 3H). LC-MS (ES+) m/z 448.94, [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-f22a5af1033b4dbda8741fc1644a9b7b |
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| Source note | uspto-grants-2012_11 |
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