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Triethylamine → HCID 13124491, compound

HRID 1603246
Notes
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Reaction equation

HRID 1603246 reaction equation
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:20]([OH:22])=O)[CH2:13]C1C=CC=CC=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([N:25](CC)CC)C.ClC(OCC)=O.[C:36]([O:39][CH2:40][CH3:41])(=[O:38])[CH3:37]>C(Cl)(Cl)Cl>[NH2:25][C@H:41]1[C@H:40]([O:39][C:36](=[O:38])[CH3:37])[NH:11][C:9]1=[O:8].[CH2:1]([O:8][C:9]([NH:11][C@H:12]1[C@H:13]([O:39][C:36](=[O:38])[CH3:37])[NH:25][C:20]1=[O:22])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
ParticipantsConditionsProcedureSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 10928Ethyl chloroformateHCID 70878Benzyloxycarbonyl-L-phenylalanine

Product 2

HCID 13124491HCID 13124491, compoundHCID 15428308HCID 15428308, compound

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Conditions

Temperature
-2.5 °C

Procedure

To a solution of N-benzyloxycarbonyl-L-phenylalanine (5.98 g, 20 mmol) and triethylamine (2.02 g, 20 mmol) in chloroform (100 ml), ethyl chloroformate (2.18 g, 20 mmol) was added at -15° C. The reaction mixture was stirred at a bath temperature of -10 to 5° C. for 1.5 hrs. Then a precooled (ca. -15° C.) solution of (3S,4S)-3-amino-4-acetoxy-azetidin-2-one in ethyl acetate, which was obtained from hydrogenation of (3S,4S)-3-benzyloxycarbonylamino-4-acetoxy-azetidin-2-one (see above), was added at -15° C. and stirring was continued at a bath temperature of -15 to 5° C. for 1 hr. After removal of solvent, the residue was dissolved in ethyl acetate, washed with water, brine and dried over sodium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography using hexane-ethyl acetate (1:2) as eluent and the title compound was obtained as white solid.

Sources & evidence

ORD record
ord-f684e75ecec0442183ea2b4d7b4c9984
Source dataset
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05986108

Reaction notes

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On this pageParticipantsConditionsProcedureSources & evidenceReaction notes