Sodium Bicarbonate → HCID 11224264, compound

HRID 2423365Notes

Reaction equation

HRID 2423365 reaction equation
Cl.C(OCC)(=O)C.[CH2:8]([O:10][C:11]([C@:13]1([NH:35]C(OC(C)(C)C)=O)[C@H:18]([NH:19][CH2:20][C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[C:23]([Cl:28])[CH:22]=2)[CH2:17][C@@H:16]2[C@H:14]1[C@@:15]2([F:34])[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[O:12])[CH3:9].C(=O)([O-])O.[Na+]>>[CH2:8]([O:10][C:11]([C@:13]1([NH2:35])[C@H:18]([NH:19][CH2:20][C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[C:23]([Cl:28])[CH:22]=2)[CH2:17][C@@H:16]2[C@H:14]1[C@@:15]2([F:34])[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[O:12])[CH3:9]

Participants

4

Reactant 3

HCID 516892Sodium BicarbonateHCID 21866389Hydrogen chloride-ethyl acetateHCID 66628528HCID 66628528, compound

Product 1

HCID 11224264HCID 11224264, compoundYield 92.3%

Procedure

2.8 mL of a 4N hydrogen chloride/ethyl acetate solution was added to 28 mg of (1R,2R,3R,5R,6R)-2-t-butoxycarbonylamino-3-(3,4-dichlorobenzylamino)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester, and the mixture was stirred for 6 hours at ice-cooling, and further stirred for 18 hours at room temperature. The reaction solution was ice-cooled, and then neutralized with a saturated aqueous solution of sodium hydrogen carbonate, followed by separation. The aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with saturated aqueous solution of sodium chloride, and then dried over anhydrous sodium sulfate. After the desiccant was filtured off, the filtrate was concentrated under reduced pressure, thereby yielding 21 mg of (1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzylamino)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester.

Workup

  1. temperaturecooling
  2. stirringfurther stirred for 18 hours at room temperature
  3. temperaturecooled
  4. customfollowed by separation
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. washwashed with saturated aqueous solution of sodium chloride
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-678be613a497415a8d5e939d14058924
Source dataset
uspto-grants-2011_06
Patent number
US07960579B2

Reaction notes

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