Реакция #2006415

Уравнение реакции

NH2OTHP

solution 41

4-[4-(Benzenesulfonylamino)-phenyl]-butyric Acid

1 -(3-Dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride

1-Hydroxybenzotriazole hydrate

10-camphorsulfonic acid

→

title compound 42

Выход 13.3%

N-Hydroxy-4-[4-(benzenesulfonylamino)-phenyl]-butanamide

Выход 13.3%

Растворители

DMF

Условия реакции

Обработка

1. 1
   ТемператураThe resulting mixture was heated at 50° C. for 24 h
2. 2
   Другоеthe DMF solvent was evaporated under reduced pressure
3. 3
   workup.DISSOLUTIONthe residue was dissolved in CH2Cl2
4. 4
   Промывкаwashed with a saturated aqueous solution of NaHCO3
5. 5
   СушкаThe combined organic extracts were dried over (MgSO4)
6. 6
   Другоеthen evaporated
7. 7
   ДругоеThe crude compound was purified by flash chromatography
8. 8
   workup.DISSOLUTIONThe residue was then dissolved in MeOH (30 mL)
9. 9
   workup.STIRRINGThe mixture was stirred 2 h at 50° C.
10. 10
    Другоеcondensed under reduced pressure at room temperature
11. 11
    ДругоеThe crude was purified by flash chromatography

Методика

To a solution 41 (800 mg, 2.59 mmol) in DMF (20 mL) at room temperature were added 1 -(3-Dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (EDC, 593 mg, 3.12 mmol), and 1-Hydroxybenzotriazole hydrate (HOBT, 524 mg, 3.89 mmol). The mixture was stirred 20 min. at room temperature then NH2OTHP (455 mg, 3.89 mmol) was added. The resulting mixture was heated at 50° C. for 24 h then the DMF solvent was evaporated under reduced pressure and the residue was dissolved in CH2Cl2, washed with a saturated aqueous solution of NaHCO3. The combined organic extracts were dried over (MgSO4) then evaporated. The crude compound was purified by flash chromatography using Hexane/acetone (7:3) as solvent mixture. The residue was then dissolved in MeOH (30 mL) then 10-camphorsulfonic acid (CSA, 300 mg, 1.30 mmol) was added. The mixture was stirred 2 h at 50° C. then the solvents were condensed under reduced pressure at room temperature to avoid thermal decomposition. The crude was purified by flash chromatography using CH2Cl2/MeOH (9:1) as solvent mixture giving the title compound 42 (115 mg, 13%) as a yellowish solid.

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