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Dicyclohexylcarbodiimide → 3-Carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acid

HRID 127095
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HRID 127095 반응식
[O:1]=[C:2]1[NH:6][C:5]([CH2:7][C:8]([OH:10])=O)=[CH:4][S:3]1.ON1C(=O)CCC1=O.C1(N=C=NC2CCCCC2)CCCCC1.[C:34]([O:37][CH2:38][C:39]1[CH2:40][S:41][C@@H:42]2[CH:49]([NH2:50])[C:48](=[O:51])[N:43]2[C:44]=1[C:45]([OH:47])=[O:46])(=[O:36])[NH2:35].C[Si](CC(N)=O)(C)C>O1CCCC1.C(OCC)(=O)C.O>[C:34]([O:37][CH2:38][C:39]1[CH2:40][S:41][C@@H:42]2[CH:49]([NH:50][C:8](=[O:10])[CH2:7][C:5]3[NH:6][C:2](=[O:1])[S:3][CH:4]=3)[C:48](=[O:51])[N:43]2[C:44]=1[C:45]([OH:47])=[O:46])(=[O:36])[NH2:35]
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참가 물질

9

반응물 5

HCID 10868DicyclohexylcarbodiimideHCID 80170N-HydroxysuccinimideHCID 357676Acetamide, 2-(trimethylsilyl)-HCID 127847593-Carbamoyloxymethyl-7-amino-3-cephem-4-carboxylic acidHCID 131325982-Oxo-2,3-dihydrothiazol-4-ylacetic acid

생성물 1

HCID 70572400
3-Carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acid
수율 5.8%

시약·촉매·용매 3

HCID 962Water용매HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

To a mixture of 2-oxo-2,3-dihydrothiazol-4-ylacetic acid (0.4 g.) and N-hydroxysuccinimide (0.3 g.) in tetrahydrofuran (15 ml.) was added N,N'-dicyclohexylcarbodiimide (0.52 g.) with stirring at room temperature, and the mixture was further stirred for 2 hours at the same temperature. Thus obtained solution was added to a solution of 3-carbamoyloxymethyl-7-amino-3-cephem-4-carboxylic acid (0.816 g.) and trimethylsilylacetamide (0.27 g.) in ethyl acetate (30 ml.) at room temperature, and the mixture was stirred for 16 hours at the same temperature. After the reaction, the reaction mixture was cooled to at -20° C., and then water (20 ml.) was added thereto. After stirring the mixture sufficiently, the mixture was filtered, and then the ethyl acetate layer was separated therefrom. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, treated with activated carbon, and then the solvent was distilled off under reduced pressure. The residue was pulverized in diethyl ether, collected by filtration and then dried to give 3-carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acid (60 mg.).

후처리

  1. stirringthe mixture was further stirred for 2 hours at the same temperature
  2. stirringthe mixture was stirred for 16 hours at the same temperature
  3. customAfter the reaction
  4. temperaturethe reaction mixture was cooled to at -20° C.
  5. stirringAfter stirring the mixture sufficiently
  6. filtrationthe mixture was filtered
  7. customthe ethyl acetate layer was separated
  8. washThe ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride
  9. dry with materialdried over magnesium sulfate
  10. additiontreated with activated carbon
  11. distillationthe solvent was distilled off under reduced pressure
  12. filtrationcollected by filtration
  13. customdried

출처 및 근거

ORD 기록
ord-5c293cd717ea436daa20727f75ed10fa
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04254260

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