HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907145Generated: November 2, 2026
Potassium Iodide → 6-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid
https://huagongshe.com/reaction/1907145
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 6-amino-5-methyl-2H-indazole-7-carboxylic acid | HCID 46855718 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid | HCID 58500429 | — |
Reaction Steps
To a suspension of 6-amino-5-methyl-1H-indazole-7-carboxylic acid (0.956 g, 5 mmol) in dimethylformamide (4 ml) was added sodium hydrogenocarbonate (0.462 g, 5.5 mmol) and the resulting mixture was stirred at 40° C. for 15 minutes before 4-methoxybenzyl chloride (0.861 g, 5.5 mmol) was introduced. A catalytic amount of potassium iodide was added and the mixture was stirred for 18 hours at that temperature. After cooling down, the crude mixture was placed on top of a silica gel column and the product was purified by flash chromatography using a gradient starting from 50% ethyl acetate-50% cyclohexane to 100% ethyl acetate, then 1% acetic acid in ethyl acetate. The fractions containing the desired compound were evaporated and the residue was triturated with diethyl ether and filtered to yield light orange crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598078B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-9d1fc43bf4a54b69a3823e96147949bf |
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| Source note | uspto-grants-2013_12 |
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