Hydrochloric Acid → HCID 86738755, compound
Reaction equation
C(OC([C:17]1[N:18]2[CH:21]([O:22][CH2:23][C:24]=1[CH:25]=[CH:26]N(C)C)[CH:20](NC(=O)C(=NOC)C1N=C(NC(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)SC=1)[C:19]2=[O:62])=O)(C1C=CC=CC=1)C1C=CC=CC=1.Cl.C(OCC)(=[O:66])C>>[O:62]=[C:19]1[N:18]2[CH:21]([O:22][CH2:23][C:24]([CH2:25][CH:26]=[O:66])=[CH:17]2)[CH2:20]1Participants
Procedure
A solution of the E form of the syn isomer of 2-benzhydryloxycarbonyl-3-(2-dimethylaminovinyl)-7-[2-methoxyimino-2-(2-tritylaminothiazol-4-yl)-acetamido]-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene (1.05 g) in ethyl acetate (10 cc) is stirred vigorously for 1 hour at 20° C., in the presence of a 1 N solution of hydrochloric acid (5 cc). The mixture is separated by decantation and the organic phase is washed with a saturated solution of sodium bicarbonate (10 cc), distilled water (10 cc) and a saturated solution of sodium chloride (10 cc). The ethyl acetate phase is dried over anhydrous magnesium sulphate and filtered and the filtrate is concentrated to dryness at 30° C. under reduced pressure (20 mm Hg; 2.7 kPa). This yields the syn isomer of 2-benzhydryloxycarbonyl-7-[2-methoxyimino-2-(2-tritylaminothiazol-4-yl)-acetamido[-8-oxo-3-(2-oxoethyl)-5-oxa-1-azabicyclo[4.2.0]-oct-2-ene (1.00 g) in the form of a hard yellow foam.
Workup
- customThe mixture is separated by decantation
- washthe organic phase is washed with a saturated solution of sodium bicarbonate (10 cc)
- distillationdistilled water (10 cc)
- dry with materialThe ethyl acetate phase is dried over anhydrous magnesium sulphate
- filtrationfiltered
- concentrationthe filtrate is concentrated to dryness at 30° C. under reduced pressure (20 mm Hg; 2.7 kPa)
Sources & evidence
- ORD record
- ord-a1b72a80c881406fa1052c2f65f68594
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04369315
Reaction notes
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