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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252492Generated: October 27, 2026

Diisopropylamine → 1-ethyl-6-methoxy-2-tributylstannanyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/252492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTributyltin iodideHCID 23765—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-ethyl-6-methoxy-1H-indole-3-carbonitrileHCID 11644100—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-ethyl-6-methoxy-2-tributylstannanyl-1H-indole-3-carbonitrileHCID 5942494998.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of THF (60 mL) and diisopropylamine (5.5 mL, 39 mmol) is cooled to −78° C. n-Butyllithium (14.5 mL, 2.5M in hexanes, 36.2 mmol) is added dropwise over 5 minutes. The LDA mixture is stirred at −78° C. for 10 minutes, and then at 0° C. for 20 minutes. The solution is re-cooled to −78° C. 1-ethyl-6-methoxy-1H-indole-3-carbonitrile (5.0 g, 25 mmol), prepared as in example 1A, is taken up in THF (30 mL) and added dropwise to the LDA mixture over 15 minutes. The reaction is stirred at −78° C. for 10 minutes, and at 0° C. for 30 minutes. Once again, the reaction mixture is cooled to −78° C. Tributyltin iodide (10 mL, 35 mmol) is added dropwise. This is stirred at −78° C. for 15 minutes, and then at 0° C. for 30 minutes. The reaction mixture is absorbed onto silica gel and concentrated. Purification by chromatography (CH2Cl2) yields 1-ethyl-6-methoxy-2-tributylstannanyl-1H-indole-3-carbonitrile (12.05 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-9a6bfe48b1e1457b9549cba4ac984fa4
Source noteuspto-grants-2011_01