HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241232Generated: October 30, 2026
Hydrazine hydrate (1:1) → (R)-2-[3-(2-aminopropyl)-1H-indol-7-yloxy]-N,N-diethyl-acetamide
https://huagongshe.com/reaction/1241232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | (R)-7-diethylaminocarbonylmethoxy-3-(2-phthalimidopropyl)indole | HCID 58713924 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-2-[3-(2-aminopropyl)-1H-indol-7-yloxy]-N,N-diethyl-acetamide | HCID 10968695 | 96% |
Reaction Steps
(R)-7-Diethylaminocarbonylmethyloxy-3-(2-phthalimidopropyl)indole 10.27 g was suspended in 100 ml of ethanol, and 2.5 ml of hydrazine monohydrate was added thereto. The suspension was heated to reflux in an oil bath of 85° C. For 3 hours. After cooling down, the resulting deposited insoluble materials were filtered off, and the filtrate was concentrated under reduced pressure. Ethyl acetate and a sodium hydroxide aqueous solution were added to the residue and distributed in liquid-liquid, and the organic layer was further washed with a sodium hydroxide aqueous solution and dried. The solution was evaporated under reduced pressure. The resulting residue was slowly crystallized, and dried under reduced pressure, whereby 6.90 g of the title compound was obtained in the form of a pale brownish white substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115412B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-aa7188ec5e114b029020b4845f5c56a1 |
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| Source note | uspto-grants-2006_10 |
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