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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907109Generated: November 1, 2026

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

https://huagongshe.com/reaction/907109

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, was heated with 1.5 mL of dimethylformamide dimethyl acetal and 100 μL pyrrolidine at 110° C. overnight. The DMF dimethyl acetal was removed in vacuo. The residue was redissolved in 3 mL of acetic acid, hydrazine hydrate (70 μL, 1.38 mmol) was added, and the mixture was heated to 100° C. for 2 h. The acetic acid was removed in vacuo, and the residue was partitioned between EtOAc and saturated NaHCO3. The organic phase was 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 gave a white crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-76fe3c556e424629a39681f0103d031e
Source noteuspto-grants-2011_09