HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066892Generated: October 30, 2026
HCID 15512201, compound → HCID 21196617, compound
https://huagongshe.com/reaction/1066892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15512201 | HCID 15512201 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21196617 | HCID 21196617 | — |
Reaction Steps
A 1.60 g of potassium hydroxide was added to an ethylene glycol (20 ml) solution containing 0.51 g of [2-(1H-furo[2,3-g]indazol-1-yl)ethyl]acetamide, and the mixture was stirred at 170° C. for 2 hours. The reaction solution was cooled, diluted with water and then extracted with ethyl acetate. The organic layers were combined, washed with water and brine and then dried over anhydrous magnesium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated and the thus obtained residue was purified by a silica gel column chromatography (eluent: chloroform/methanol =95/5) to give 2-(1H-furo[2,3-g]indazol-1-yl)ethylamine. The thus obtained 2-(1H-furo[2,3-g]indazol-1-yl)ethylamine was dissolved in a mixture of ethanol and ethyl acetate, 4 N hydrochloric acid ethyl acetate solution was added to the resulting solution, and the resulting crystals were collected by filtration and dried under a reduced pressure to give 0.06 g of 2-(1H-furo[2,3-g]indazol-1-yl)ethylamine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245796B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-eaf26ce403424059ba8b5eb9433da857 |
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| Source note | uspto-grants-2001_06 |
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