| Identification | Back Directory | [Name]
[6R-[6alpha,7beta(Z)]]-3-[[(Aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-pentenyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid compd. with N-(1-methylethyl)-2-propanamine | [CAS]
153012-37-4 | [Synonyms]
BPCM
BCN、BPCM
Boc-Cefcapene
Boc-Cefcapene/BCN
Boc-Cefcapene.DIPA
Cefcapene Impurity 8
Cefcapene InterMediate
Intermediate of Cefcapene
[6R-[6alpha,7beta(Z)]]-3-[[(Amin
Cephalosporin diisopropylamine salt
N-Boc Cefcapene N,N-DiisopropylaMine
precursor of cefcapene diisopropylanmine
Precursor of cefcapene diisopropylanmine salt
[6R-[6alpha,7beta(Z)]]-3-[[(Aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-di
(6R,7R)-7-[(Z)-2-(2-t-Butoxycarbonylaminothiazol-4-yl)pent-2-enoylamino]-3-carbamoyloxy -methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diisopropylamine salt
(6R,7R)-7-[[(Z)-2-(2-t-Butoxycarbonylaminothiazol-4-yl)-2-pentenoyl]amino]-3-aminocarbonyl-oxymethyl-8-oxo-5-thia-1-azabicylo[4.2.0]oct-2-ene-2-carboxylic acid diisopropylamine salt
diisopropylamine 7-((2-(2-(2-(tert-butoxy)-2-oxoethyl)thiazol-4-yl)-1-oxidopent-2-en-1-ylidene)amino)-3-((iminooxidomethoxy)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
[6R-[6alpha,7beta(Z)]]-3-[[(Aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-pentenyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid compd. with N-(1-met
[6R-[6alpha,7beta(Z)]]-3-[[(Aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-pentenyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid compd. with N-(1-methylethyl)-2-propanamine
[6R-[6alpha,7beta(Z)]]-3-[[(Aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxChemicalbooko-2-pentenyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacidcompd.withN-(1-methylethyl)-2-propanamine USP/EP/BP | [EINECS(EC#)]
604-880-2 | [Molecular Formula]
C29H43N5O8S2 | [MDL Number]
MFCD31382339 | [MOL File]
153012-37-4.mol | [Molecular Weight]
653.81 |
| Questions And Answer | Back Directory | [Preparation]
Precursor of cefcapene diisopropylanmine salt (BCN) is an important intermediate in the synthesis of cefcardine hydrochloride. Starting with 7-aminocephalosporanic acid, it undergoes hydrolysis to yield 3-deacetyl-7-aminocephalosporanic acid, which is then reacted with (Z)-2-(2-tert-butoxycarbonylaminothiazol-4-yl)-2-pentenoic acid and diisopropylamine to obtain Precursor of cefcapene diisopropylanmine salt. The overall yield is over 70%, and the purity is over 98%. |
| Hazard Information | Back Directory | [Description]
The precursor of Boc-Cefcapene(BCN) is a key intermediate in the synthesis of Cefcapene. Cefcapene is a fourth generation cephalosporin antibiotic, which introduces protective groups on its side chain amino group and the carboxyl group of the cephalosporin nucleus to obtain the precursor of Boc-Cefcapene(BCN). After modification of the BCN, various Cefcapene drugs can be obtained. | [Chemical Properties]
Yellowish crystalline powder. | [Uses]
N-Boc Cefcapene N,N-Diisopropylamine is a precursor of Cefcapene N,N-Diisopropylamine. |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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