HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884780Generated: October 30, 2026
Hydrochloric Acid → 3-[5-Amino-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-imidazole-4-carbonyl]-benzoic acid
https://huagongshe.com/reaction/884780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 3-iodobenzoate | HCID 18386959 | — |
| Reactant | HCID 58088961 | HCID 58088961 | — |
| Reactant | HCID 178478990 | HCID 178478990 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[5-Amino-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-imidazole-4-carbonyl]-benzoic acid | HCID 58089033 | — |
Reaction Steps
To a solution of 3-iodobenzoic acid tert-butyl ester (4.6 g) in THF (20 mL) at −40° C. under N2 was added cyclohexylmagnesium chloride (2M in THF, 8.5 mL). The solution was kept at −40° C. to 0° C. for 20 min., when 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide was added and the reaction was kept at rt for 1 h. Then HCl (4 M, 10 mL) was added and the mixture was heated at 40 to 45° C. overnight. The mixture was neutralized with K2CO3 solution and extracted with EtOAc (2×100 mL) and the combined organics dried over Na2SO4, and concentrated. Purification of the crude product by column chromatography (EtOAc: MeOH=6:1) gave the desired product (0.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242117B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-a3a7e4be07314d2caebd98d480fe6944 |
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| Source note | uspto-grants-2012_08 |
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