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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956183Generated: October 31, 2026

Hydrochloric Acid → HCID 23227007, compound

https://huagongshe.com/reaction/1956183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantMethyl isobutyrateHCID 11039—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 23226983HCID 23226983—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 23227007HCID 23227007—

Reaction Conditions

Temperature12 °C

Reaction Steps

To a solution of lithium diisopropylamide prepared from 5.3 g (57 mmol) of diisopropylamine and 21 mL (57 mmol) of 2.5M n-butyl lithium in hexane and 100 mL of dry tetrahydrofuran at -10° C. was slowly added with stirring 5.3 g (57 mmol) of methyl 2-methylpropanoate. The resulting solution was allowed to warm slowly to 12° C. and was then recooled to -10° C. To this was added in small portions with stirring 7.0 g (26 mmol) of 5-(chloro-(2-fluorophenyl)methyl)-4-methylthiopyrimidine. After 1 hr the resulting solution was warmed to ambient temperature. Ether and dilute aqueous hydrochloric acid were added and the ethereal phase was recovered, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography on silica gel to obtain 5.3 g (60 of theory) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780465
Source datasetuspto-grants-1998_07
ORD IDord-befbf5c1f39c4e3299b46d5c6f9b4b1e
Source noteuspto-grants-1998_07