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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1012912Erstellt: 24. Oktober 2026

Water → [4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester

https://huagongshe.com/de/reaction/1012912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzothiazoleHCID 7222—
EduktButyllithiumHCID 178418339—
EduktHCID 178502731HCID 178502731—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl esterHCID 6731716682,1%

Reaktionsschritte

To a solution of benzothiazole (675 mg, 0.55 ml, 5 mmol) in THF (20 ml) at −78° C. was added dropwise n-BuLi (2.5M in Hex, 2 ml) such that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of [trans-4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (716 mg, 2.5 mmol, prepared according to WO 03/053933) in THF (2 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). Mixture was poured into water and extracted with EtOAc. The combined organic extracts were washed with brine and dried over MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography over SiO2 (Hex/EtOAc 4:1 then DCM). The relevant fractions were pooled, evaporated under reduced pressure, digested with Hex and filtered to give 740 mg (82%) of [4-(benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07981886B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-35a01e6be0c24725a8d37793c2468181
Quellennotizuspto-grants-2011_07