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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391331Erstellt: 24. Oktober 2026

Methyl iodide → HCID 59578436, Verbindung

https://huagongshe.com/de/reaction/391331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt3-Bromo-4-chloropyridineHCID 817696—
EduktLithium diisopropylamideHCID 2724682—
EduktN-(cyclopropylmethylene)methanesulfonamideHCID 66788560—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59578436HCID 59578436—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of DIPA (1.71 mL, 12 mmol) in THF (50 mL) at −78° C. was added 1.6M BuLi (7.5 mL, 12.0 mmol) and the mixture was stirred at −78° C. for 2 h. The LDA solution was cannulated into a solution of 3-bromo-4-chloropyridine (2.117 g, 11 mmol) in THF (50 mL) at −78° C., and the mixture was stirred at −78° C. for 1 h. A solution of N-(cyclopropylmethylene)methanesulfonamide (10 mmol, crude mixture) in THF (50 mL) was added and the mixture was stirred at −78° C. for 1 h. A solution of MeI (0.625 mL, 10 mmol) in THF (10 mL) was added, and the mixture was warmed to room temperature and stirred overnight. Water (0.5 mL) was added and the mixture was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with a 0-50% EtOAc-heptane gradient to give N-((5-bromo-4-chloropyridin-3-yl)(cyclopropyl)methyl)-N-methylmethanesulfonamide. MS (ESI): m/z 353.0, 355.0 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383827B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-4d2480c9553a40798ecae9f1c0e51ad7
Quellennotizuspto-grants-2013_02