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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396362Generated: October 29, 2026

Diisopropylamine → HCID 178503449, compound

https://huagongshe.com/reaction/396362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Methyl-2-(methylsulfanyl)pyrimidineHCID 821261—
Reactant4-Fluoro-N-methoxy-N-methylbenzamideHCID 14069347—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductHCID 178503449HCID 17850344965%

Reaction Steps

n-BuLi (10 ml of a 1.6 M solution in hexane; 12 mmol) is added at −78° C. to a solution of diisopropylamine (2.48 ml; 17 mmol) in THF (15 ml) and stirred for 5 min. 4-Methyl-2-(methylthio)pyrimidine (2 g; 14.5 mmol) dissolved in THF (2 ml) is added dropwise and stirred for 30 min at −78 C. 4-Fluoro-N-methoxy-N-methylbenzamide (2.66 g; 14.5 mmol) is dissolved in THF (3 ml) and added slowly to the reaction mixture. The mixture is warmed to r.t. within 45 min. and poured on water and extracted with ethyl acetate three times. The combined organic phases are dried over Na2SO4 and evaporated to dryness to yield 2.5 g (65%) of yellow crystals after recrystallisation from tert.butyl methyl ether/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608072B1
Source datasetuspto-grants-2003_08
ORD IDord-88b971d610324d35b96afbbfa5bc4890
Source noteuspto-grants-2003_08