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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518984Generated: November 4, 2026

Ethanol → HCID 86685007, compound

https://huagongshe.com/reaction/1518984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrazineHCID 9321—
ReactantHCID 86685008HCID 86685008—
SolventDichloromethaneHCID 6344—
ProductHCID 86685007HCID 8668500750%

Reaction Conditions

Temperature25 °C

Reaction Steps

N-phthaloyl protected 5-nonyloxy-4-azaindole (20 mg, 0.05 mmole) and hydrazine (3 mg, 0.09 mmole) was dissolved in CH2Cl2 (0.5 mL) in a 25 mL round bottom flask. EtOH (1 mL) was added to the reaction mixture and allowed to stir overnight at 25° C. for 12 h, after which it was cooled to 0° C., and filtered, and the white solid material was washed with 3 mL of cold CH2Cl2. The filtrate was evaporated under reduced pressure to afford 7 mg (50%) of 2-aminoethyl-5-nonyloxy-4-azaindole as a yellow solid. LRMS (ESI): M+1 for C18H29N3O calcd 304.4. found 304.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073851B2
Source datasetuspto-grants-2015_07
ORD IDord-152469a419f54f7e9dcbf9cc3ad278b4
Source noteuspto-grants-2015_07