2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate CA

Introduction:Basic information about 2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate CA, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate Basic information

Product Name:2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate
Synonyms:2-MERCAPTOBENZOTHIAZOLYL-(Z)(2-AMINOTHIAZOLE-4YL)-2-(TERT-BUTOXYCARBONYL)ISOPROPOXYIMINO ACETATE;S-2-BENZOTHIAZOYL-(Z)-2-(1-TERT-BUTOXYCARBONYL-1-METHYLETHOXYIMINO)-2-(AMINOTHIAZOL-4-YL)ACETATE;S-2-BENZOTHIAZOLYL-(Z)-2-(TERT-BUTOXYCARBONYL-ISOPROPOXYIMINO)THIOACETATE BENZOTHIAZOLE ESTER;S-2-BENZOTHIAZOLYL (Z)-2-(2-AMINOTHIAZOL-4-YL)-2-(1-T-BUTOXYCARBONYL-1-METHYL)ETHOXYIMINOTHIOACETATE;S-2-BENZOTHIAZOLYL-(2)-2-(1-TERBATOXYCANBONYL-1-METHYLETHOXYIMINO)-4-THIAZOLE ACETATE;(Z)-TERT-BUTYL 2-(1-(2-AMINOTHIAZOL-4-YL)-2-(BENZO[D]THIAZOL-2-YLTHIO)-2-OXOETHYLIDENEAMINOOXY)-2-METHYLPROPANOATE;S-2-benzothiazoyl-(Z)-2-(1-ter-butoxycanbonyl-1-methylethoxyimino)-4-thiazoleacetate;S-2-Benzothiazoyl-(Z)-2-(ter-butoxycarbonyl-isopropoxyimino)-4-thiazoleacetate(TAEM)
CAS:89604-92-2
MF:C20H22N4O4S3
MW:478.61
EINECS:419-040-9
Product Categories:Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Pharmaceutical Intermediates
Mol File:89604-92-2.mol

2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate Chemical Properties

Melting point 138-140°C
Boiling point 621.6±61.0 °C(Predicted)
density 1.41±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform, Methanol
form Solid
pka0.83±0.10(Predicted)
color Pale Yellow
InChIInChI=1S/C20H22N4O4S3/c1-19(2,3)27-16(26)20(4,5)28-24-14(12-10-29-17(21)22-12)15(25)31-18-23-11-8-6-7-9-13(11)30-18/h6-10H,1-5H3,(H2,21,22)/b24-14-
InChIKeyRCZJVHXVCSKDKB-OYKKKHCWSA-N
SMILESC(OC(C)(C)C)(=O)C(O/N=C(/C1=CSC(N)=N1)\C(SC1=NC2=CC=CC=C2S1)=O)(C)C
CAS DataBase Reference89604-92-2(CAS DataBase Reference)

Safety Information

Risk Statements 53
Safety Statements 61

2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate Usage And Synthesis

Chemical PropertiesPale Yellow Solid
UsesAn intermediate for the preparation of cephalosporin derivatives.
Synthesis

120-78-5

86299-47-0

89604-92-2

Synthesis of (Z)-2-(((1-(2-aminothiazol-4-yl)-2-((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)acetic acid from dibenzothiazole disulfide and (Z)-2-((2-(2-aminothiazol-4-yl)-2-(benzo[d]thiazol-2-ylthio)-2-oxoethylidene)amino)oxy) The general procedure for tert-butyl -2-methylpropanoate was as follows: 35 g of (Z)-2-(2-aminothiazol-4-yl)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2- yl)oxy)imino)acetic acid and 48 g of dibenzothiazole disulfide were added to a solvent mixture of dichloromethane and acetonitrile at 21 °C. (the total mass of the solvent mixture was 250 g, the density of 1.0 g/cm3). After stirring for 10 minutes, 1.0 mL of pyridine was added. At 22°C, 8.0 mL of triethylamine was slowly added. After addition, the reaction temperature was raised to 30°C and kept at this temperature for 50 minutes. Subsequently, the reaction mixture was cooled to 21 °C, and 28 mL of triethyl phosphite was slowly added dropwise at this temperature, with the dropwise addition process controlled to be completed within 2.5 hours. After the dropwise addition was completed, the reaction solution was continued at 21±1 °C for 3.0 hours. After that, the reaction mixture was cooled to 3°C and kept at this temperature for 30 minutes. Upon completion of the reaction, filtration was carried out, the solid product was collected and dried at 60 °C to afford the target product (Z)-tert-butyl 2-(((1-(2-aminothiazol-4-yl)-2-(benzo[d]thiazol-2-ylsulfanyl)-2-oxoethylidene)amino)oxy)-2-methylpropanoate in 92.6% yield and 99.3% purity.

References[1] Patent: CN106699683, 2017, A. Location in patent: Paragraph 0028-0033

2-Mercaptobenzothiazolyl-(Z)-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonyl) isopropoxyiminoacetate Preparation Products And Raw materials

Raw materialsTriethylamine-->2,2'-Dithiobis(benzothiazole)-->(Z)-2-Amino-alpha-[1-(tert-butoxycarbonyl)]-1-methylethoxyimino-4-thiazolacetic acid-->Triethyl phosphite-->Pyridine
Preparation ProductsAztreonam
2-Mercaptobenzothiazole CAS 149-30-4
2-Mercaptoethanol CAS 60-24-2
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