ChemicalBook--->CAS DataBase List--->104146-10-3

104146-10-3

104146-10-3 Structure

104146-10-3 Structure
IdentificationMore
[Name]

GCLE
[CAS]

104146-10-3
[Synonyms]

4-methoxybenzyl 3-chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate
7-PHENYLACETAMIDE-3-CHLOROMETHYL-3-CEPHEM-4-CARBOXYLIC ACID P-METHOXYBENZYL ESTER
7-PHENYLACETAMIDE-3-CHLOROMETHYL-CEPHALOSPORANIC ACID P-METHOXYBENZYL ESTER
7-PHENYLACETAMIDO-3-CHLOROMETHYL-3-CEPHEM-4-CARBOXYLIC ACID 4-METHOXYBENZYL ESTER
7-PHENYLACETAMINO-3-CHLOROMETHYL-3-CEPHEM4-CARBOXYLIC ACID P-METHOXYBENZYL ESTER
GCLE
(4-methoxyphenyl)methylester,(6r-trans)-7-((phenylacetyl)amino)
2,0)oct-2-ene-2-carboxylicacid,3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo(
7-phenylacetamido-3-chloromethylcephem-4-carbonicacidp-methoxybenzylester
7-Phenylacetamide-3-chlorormethyl-3-cepham-4-carboxylic acid P-m-ethoxybenzyl es
GCLE:INTERMEDIATE FOR CEPHALOSPORIN
7-PHENYLACETAMIDE-3-CHLORORMETHYL-3-CEPHAM-4-CARBOXYLIC ACID P-METH-OXYBENZYL ESTER
GCLE7-PHENYLACETAMIDE-3-CHLORORMETHYL-3-CEPHAM-4-CARBOXYLIC ACID P-METH-OXYBENZYL-ESTER
7-PHENYLACETAMIDO-3-CHLOROMETHYLCEPHEM-4-CARBONICACID-PARA-METHOXYBENZYLESTER
[EINECS(EC#)]

403-040-0
[Molecular Formula]

C24H23ClN2O5S
[MDL Number]

MFCD00191253
[Molecular Weight]

486.97
[MOL File]

104146-10-3.mol
Chemical PropertiesBack Directory
[Melting point ]

153-155°C
[Boiling point ]

756.6±60.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[solubility ]

Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
[form ]

Solid
[pka]

13.61±0.60(Predicted)
[color ]

White to Off-White
[Optical Rotation]

Consistent with structure
[InChIKey]

KFCMZNUGNLCSJQ-NFBKMPQASA-N
[SMILES]

N12[C@@]([H])([C@H](NC(CC3=CC=CC=C3)=O)C1=O)SCC(CCl)=C2C(OCC1=CC=C(OC)C=C1)=O
[CAS DataBase Reference]

104146-10-3(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)
GHS08
[Signal word ]

Danger
[Hazard statements ]

H334-H317
[Precautionary statements ]

P261-P285-P304+P341-P342+P311-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
[RTECS ]

XI0369883
[HS Code ]

2941.90.3000
[REACH Registrations]

Active
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

A key intermediate of cephem compounds.
[Synthesis]

1-Azetidineacetic acid, α-[1-(chloromethyl)ethenyl]-2-(2,2-dioxido-2-phenyldithio)-4-oxo-3-[(2-phenylacetyl)amino]-, (4-methoxyphenyl)methyl ester, (αR,2R,3R)-

131903-39-4

GCLE

104146-10-3

The general procedure for the synthesis of (6R,7R)-3-(chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thiophene-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid-4-methoxybenzyl ester, using the compound (CAS:131903-39-4) as a starting material, was as follows: in 2000 mL dioxane, 120 g of sodium bicarbonate ( 1.43 mol) and 200 g of azodioxanone sulfinic acid intermediate (0.336 mmol) and stirred at 10 to 15 °C. 30 g of chlorine gas (0.422 mol) was slowly passed for about 3 h. The reaction progress was monitored by HPLC until the peak area of the feedstock dropped below 0.5%. The passage of chlorine gas was stopped, sodium bicarbonate was removed by filtration and dioxane was recovered under vacuum. 2000 mL of methanol was added to dissolve the residue and the reaction temperature was maintained at 0-5 °C. Subsequently, a 900 mL methanol solution of 18 g sodium methanolate (0.34 mol) was added and the reaction was maintained at 0~5 °C for 30 min. The pH of the reaction system was adjusted to 4~6 with 10% hydrochloric acid and stirring was continued at 0~5°C for 1 hour. After completion of the reaction, the product was collected by filtration, washed with water and methanol sequentially, and dried to give 125 g of GCLE in 76.3% yield and ≥94% purity.

[References]

[1] Patent: CN107033162, 2017, A. Location in patent: Paragraph 0024; 0027
Spectrum DetailBack Directory
[Spectrum Detail]

GCLE(104146-10-3)1HNMR
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