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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163063Generated: October 28, 2026

Ethanol → HCID 22508891, compound

https://huagongshe.com/reaction/1163063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-5-methylpyrrolo[2,1-f][1,2,4]triazine-6-carboxylateHCID 24823948—
SolventDichloromethaneHCID 6344—
ProductHCID 22508891HCID 2250889163%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of 4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-5-methyl-pyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acid ethyl ester (68 mg 0.19 mmol) in anhydrous methylene chloride (2.0 mL) at −78° C. under argon was added DIBAL (0.48 mmol, 0.48 mL, 1.0M, 2.5 eq.) dropwise. After 5 minutes, the mixture was warmed to −15° C. and allowed to stir for an additional 15 minutes. A drop of ethanol was added to quench the reaction followed by 1N sodium hydroxide (0.2 mL) and 1.0 mL of ethyl acetate and 1.0 mL of THF. After 30 minutes, the mixture was filtered to remove the resulting solid. The filtrate was dried, concentrated in vacuo, and chromatographed using silica gel eluting with 40-75% ethyl acetate in hexanes (gradient). Concentration of the desired fractions afforded the title compound (39 mg, 63%) as a clear oil. LC/MS; (M+H)+=327.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820814B2
Source datasetuspto-grants-2010_10
ORD IDord-2ece5d6ba7d14e4baa0157eb53425e9d
Source noteuspto-grants-2010_10