Реакция #88920

Уравнение реакции

Intermediate 53a

5-tert-Butyl-2-{4-chloro-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-ylamine

sodium hydroxide

2,2,2-trichloroethyl chloroformate

→

title compound

Выход 101.0%

(5-tert-Butyl-2-{4-chloro-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-carbamic acid 2,2,2-trichloro-ethyl ester

Выход 101.0%

Растворители

EtOAc

Условия реакции

Обработка

1. 1
   ЭкстракцияThe aqueous layer was extracted with EtOAc (2×10 mL)
2. 2
   Другоеthe combined organics dried
3. 3
   Концентрированиеconcentrated in vacuo
4. 4
   ДругоеThe residue was purified by FCC

Методика

To a solution of Intermediate 53a (445 mg, 1.13 mmol) in EtOAc (4 mL) and 1N sodium hydroxide solution (2.40 mL, 2.40 mmol) was added 2,2,2-trichloroethyl chloroformate (165 μL, 1.20 mmol), and the mixture stirred vigorously at RT for 1.5 h. The aqueous layer was extracted with EtOAc (2×10 mL), and then the combined organics dried and concentrated in vacuo. The residue was purified by FCC, using 0-30% EtOAc in cyclohexane, to give the title compound (650 mg, 100%). LCMS (Method 3): Rt 4.90 min, m/z 568, 570, 572 [MH+].

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