Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20094534 | HCID 20094534 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20094536 | HCID 20094536 | 75% |
Reaction Steps
Ethanol (1.2 ml ), ion-exchanged water (0.3 ml ), and potassium hydroxide (28 mg) were added to 2-butyl4-chloro-1-[3-bromo-2- (2-ethoxycarbonylphenyl)-2H-indazol-5-yl]methyl-1 H-imidazole-5-carbaldehyde (101 mg, 0.186 mmol) as obtained in Example 1, and the mixture was stirred at room temperature for one day. The mixture was concentrated in an evaporator, and partitioned by ion-exchanged water (2.5 ml) and diethyl ether (5 ml). The water layer was separated and conc. hydrochloric acid was dropwise added thereto to adjust its pH to 5. The resultant solid was filtered off and washed three times with ion-exchanged water (1 ml). The solid was dried in vacuo overnight at 37° C. to give 72 mg of 2-butyl-4-chloro-1-[3-bromo-2-(2-carboxyphenyl)-2H-indazol-5-yl]methyl-1H-imidazole-5-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387684 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-54abfc4d2f234f5ca26b2ded46ba518f |
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| Source note | uspto-grants-1995_02 |
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