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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216424Erstellt: 25. Oktober 2026

N-bromobutanimide → HCID 178497004, Verbindung

https://huagongshe.com/reaction/216424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
EduktMeOH tetrahydrofuranHCID 21899815—
EduktHCID 178497005HCID 178497005—
LösungsmittelMethanolHCID 887—
ProduktHCID 178497004HCID 17849700479,2%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

7-Fluoro-6-o-tolylamino-1H-benzoimidazole-5-carboxylic acid methyl ester 7a (2.00 g, 6.68 mmol) is suspended in 1:1 THF/MeOH (60 mL) and cooled to −78° C. under a nitrogen atmosphere. A solution of NBS (1.20 g, 6.75 mmol) in 1:1 THF/MeOH (5 mL) is added followed by a MeOH (5 mL) solution of TsOH.H2O (1.9 g, 10.0 mmol). After 30 minutes, the reaction mixture is warmed to 0° C. and then after 1 hour warmed to room temperature. After 16 hours, more NBS (0.12 g, 0.67 mmol) is added and the reaction mixture is allowed to stir for 3 hours. The reaction mixture is quenched by the addition of 10% Na2S2O4 solution. After 30 minutes, the reaction mixture is diluted with water and ethyl acetate and the layers separated. The aqueous layer is extracted with ethyl acetate. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The recovered solid is triturated with methylene chloride to give 2.00 g (79%) pure desired product: MS APCI (+) m/z 380, 378 (M+1 Br pattern) detected.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193229B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-7935da8db73540339a4c3f57d9c6b224
Quellennotizuspto-grants-2012_06