HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993598Generated: October 25, 2026
Sodium Hydroxide → 5-((6-Chloropyrimidin-4-yl)oxy)-1H-indole
https://huagongshe.com/reaction/1993598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Hydroxyindole | HCID 16054 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-((6-Chloropyrimidin-4-yl)oxy)-1H-indole | HCID 57455156 | — |
Reaction Steps
To a mixture of NaOH (720 mg, 18 mmol) and acetone/water 1:1 (72 ml), 4,6-dichloropyrimidine (2.4 g, 18 mmol) and 5-hydroxy-indole (2.68 g, 18 mmol) are added. After stirring for 70 min at 65° C., the brownish solution is cooled to rt and diluted with AcOEt and water. The aqueous layer is separated off and extracted twice with AcOEt. The organic layers are washed with water, saturated Na2CO3 solution, water and brine, dried (Na2SO4) and concentrated. The crude product can be used without further purification: m.p.: 137-138° C.; MS: [M+1]+=246.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652022B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-fda71291314b4954ab91941c4e258e26 |
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| Source note | uspto-grants-2010_01 |
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