HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107532Generated: October 30, 2026
HCID 15054039, compound → HCID 23046050, compound
https://huagongshe.com/reaction/2107532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15054039 | HCID 15054039 | — |
| Reactant | 1-(Diphenylmethyl)-3-(2-oxiranylmethoxy)azetidine | HCID 15165710 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23046050 | HCID 23046050 | — |
Reaction Steps
8.8 g of 4-hydroxy-1H-indole-2-carboxamide are dissolved in 250 ml of 0.8 percent strength sodium hydroxide solution and a solution of 16.3 g of 1-(diphenylmethyl)-3-(2,3-epoxypropoxy)azetidine in 250 ml of dioxane is added. The mixture is allowed to stand for 4 hours at room temperature and then warmed to 60° C. for a further 20 hours. The reaction mixture is then stirred into 1 l of ice water and extracted twice with 500 ml of methylene chloride each time. The organic phase is dried using potassium carbonate and the solvent is removed by distillation in vacuo. The residue is triturated twice with 100 ml of diisopropyl ether each time and filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935414 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-edefa76a539746cda0badd02eb6ba026 |
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| Source note | uspto-grants-1990_06 |
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