Sodium Acetate → HCID 58484956, compound

HRID 1255437Notes

Reaction equation

HRID 1255437 reaction equation
[CH:1]([C:3]1([C:6]([O:8][CH3:9])=[O:7])[CH2:5][CH2:4]1)=O.Cl.[F:11][C:12]1([F:18])[CH2:16][CH2:15][C@@H:14]([NH2:17])[CH2:13]1.C([O-])(=O)C.[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[F:11][C:12]1([F:18])[CH2:16][CH2:15][C@@H:14]([NH:17][CH2:1][C:3]2([C:6]([O:8][CH3:9])=[O:7])[CH2:5][CH2:4]2)[CH2:13]1

Participants

6

Procedure

Methyl 1-formylcyclopropanecarboxylate (45% w/w, 3.205 g, 11.26 mmol) and (R)-3,3-difluorocyclopentanamine hydrochloride (1.774 g, 11.26 mmol) were dissolved in dichloromethane (20 mL) at 0° C. under nitrogen. To this solution was added sodium acetate (0.923 g, 11.26 mmol) followed by sodium triacetoxyborohydride (3.46 g, 16.32 mmol). The reaction mixture was allowed to warm up to room temperature overnight. The reaction mixture was quenched with a saturated aqueous solution of sodium bicarbonate and stirred at room temperature for a further 10 minutes. The aqueous layer was extracted 3 times with dichloromethane. The combined organic layers were washed with brine, dried over magnesium sulfate and concentrated under vacuo. The residue was purified on silica gel by flash column chromatography to give the required compound (2.631 g, quantitative yield).

Workup

  1. customThe reaction mixture was quenched with a saturated aqueous solution of sodium bicarbonate
  2. extractionThe aqueous layer was extracted 3 times with dichloromethane
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under vacuo
  6. customThe residue was purified on silica gel by flash column chromatography

Sources & evidence

ORD record
ord-f763dd17202e4e829bc0a431251a7510
Source dataset
uspto-grants-2013_06
Patent number
US08461149B2

Reaction notes

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