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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369408Generated: October 31, 2026

Diisopropylamine → HCID 178503449, compound

https://huagongshe.com/reaction/1369408

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

nBuLi (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 mm 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 numberUS06579874B2
Source datasetuspto-grants-2003_06
ORD IDord-b78919cabc5d45dc80ee2862df945bac
Source noteuspto-grants-2003_06