HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808571Generated: October 27, 2026
Potassium Hydroxide → HCID 58054524, compound
https://huagongshe.com/reaction/1808571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(Chloromethyl)benzamide | HCID 458363 | — |
| Reactant | 4-Methoxy-1H-indazol-3-amine | HCID 18526053 | — |
| Reactant | HCID 86661402 | HCID 86661402 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58054524 | HCID 58054524 | 80% |
Reaction Steps
To a solution of 4-(methyloxy)-1H-indazol-3-amine (for a preparation see Intermediate 1) (0.816 g, 5 mmol) in DMSO (50 mL) at room temperature under nitrogen was added potassium hydroxide (0.561 g, 10.0 mmol). After stirring the resulting deep red solution for 25 min 4-(chloromethyl)benzamide (0.848 g, 5.00 mmol) was added in one portion. The reaction mixture was stirred for a further 30 min and then poured into water (250 mL), forming an emulsion. The reaction mixture was extracted using chloroform (3×250 mL). The combined organic solutions were washed with water (250 mL) and passed through hydrophobic frit. The solvent was removed in vacuo and the residue was loaded in dichloromethane to a silica (100 g) cartridge and purified by chromatography on Flashmaster eluting with 0-100% ethyl acetate-cyclohexane+0-20% methanol-ethyl acetate over 60 min. The appropriate fractions were combined and evaporated in vacuo to give the title compound (1.18 g, 80%). LCMS: (System A) RT=0.69 min, ES+ve m/z 297 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357716B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a16f704e027248808cd6d67c03378fe5 |
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| Source note | uspto-grants-2013_01 |
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