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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009538Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 11680306, compound

https://huagongshe.com/reaction/1009538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHCID 59425473HCID 59425473—
ReactantHCID 59425954HCID 59425954—
SolventPyrrolidineHCID 31268—
ProductHCID 11680306HCID 1168030654%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(1-Ethyl-6-methoxy-1H-indol-3-yl)-ethanone (100 mg, 0.46 mmol), prepared from 1-ethyl-6-methoxy-1H-indole by the procedure described in example 1L, is heated with 1.5 mL of dimethylformamide dimethyl acetal and 100 μL pyrrolidine at 110° C. overnight. The DMF dimethyl acetal is removed in vacuo. The residue is redissolved in 3 mL of acetic acid, hydrazine hydrate (70 μL, 1.38 mmol) is added, and the mixture is heated to 100° C. for 2 h. The acetic acid is removed in vacuo, and the residue is partitioned between EtOAc and saturated NaHCO3. The organic phase is dried and concentrated and the product purified by silica gel chromatography (EtOAc/Hex, 1/1) to give 59 mg of 1-ethyl-6-methoxy-3-(2H-pyrazol-3-yl)-1H-indole (54%) as a colorless semisolid. Trituration in Et2O gives a white crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-b78920d80dd64063991a18c6e3126d59
Source noteuspto-grants-2011_07