((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate CAS 144163-97-3

Introduction:Basic information about ((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate CAS 144163-97-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate Basic information

Product Name:((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate
Synonyms:5-(p-NitrophenoxycarbonyloxyMethyl);[(5-Thiazol)Methyl]-(4-nitrophenyl)carbonate;((5-thiazolyl)Methyl)-(4-nitrophenyl)carbonate (SC);NCT;4-Nitrophenyl (thiazol-5-ylMethyl) carbonate;((5-Thiazolyl)methyl)-(4-nitrophenyl)carbote;carbonic acid 4-nitrophenyl 5-thiazolylmethyl ester;RITONAVIR INTERMEDIATE-A THIOZOLE [CARBONIC ACID-4NITROPHENYL-5-THIAZOLYLMETHYLESTER (NCT)
CAS:144163-97-3
MF:C11H8N2O5S
MW:280.26
EINECS:680-587-3
Product Categories:Heterocyclic Compounds;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Ritonavir;API intermediates
Mol File:144163-97-3.mol

((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate Chemical Properties

Melting point 65-67°C
Boiling point 475.3±45.0 °C(Predicted)
density 1.485
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility Chloroform, Ethyl Acetate (Slightly)
form Solid
pka1.86±0.10(Predicted)
color Pale Yellow
InChIInChI=1S/C11H8N2O5S/c14-11(17-6-10-5-12-7-19-10)18-9-3-1-8(2-4-9)13(15)16/h1-5,7H,6H2
InChIKeyFTEKBGGQRNJIPQ-UHFFFAOYSA-N
SMILESC(OCC1SC=NC=1)(=O)OC1=CC=C([N+]([O-])=O)C=C1
CAS DataBase Reference144163-97-3(CAS DataBase Reference)

Safety Information

((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate Usage And Synthesis

Chemical PropertiesPale-Yellow Solid
UsesRetinovir intermediate.
Synthesis

38585-74-9

5070-13-3

144163-97-3

General procedure for the synthesis of ((5-thiazolyl)methyl)-(4-nitrophenyl)carbonate (compound 9) from 5-hydroxymethylthiazole (compound 8, 17 mmol) and bis(p-nitrophenyl)carbonate (compound 7, 19 mmol): compound 7 was added to a dichloromethane (DCM, 40 mL) solution of compound 8, followed by triethylamine (26 mmol) . The reaction mixture was stirred at room temperature for 12 h. After completion of the reaction it was concentrated under reduced pressure. The concentrated mixture was diluted with ethyl acetate (EtOAc) and washed sequentially with saturated aqueous sodium carbonate (Na2CO3) solution, water and brine. After washing, the organic solvent was removed under reduced pressure. The residue was purified by fast column chromatography (silica gel as stationary phase, eluent ratio hexane/ethyl acetate=1/1) to give the final compound 9 (4.7 g).

References[1] Patent: WO2008/10921, 2008, A2. Location in patent: Page/Page column 188-189
[2] Patent: US2010/256366, 2010, A1. Location in patent: Page/Page column 19
[3] Patent: EP2231628, 2015, B1. Location in patent: Paragraph 0878
[4] Patent: US2018/30043, 2018, A1. Location in patent: Paragraph 0163

((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate Preparation Products And Raw materials

Raw materials5-Hydroxymethylthiazole-->BIS(4-NITROPHENYL) CARBONATE-->Triethylamine-->Dichloromethane
Preparation Productsthiazol-5-ylmethyl ((2R,5R)-5-amino-1,6-diphenylhexan-2-yl)carbamate
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(-)-8-[(S)-2,3-Dihydroxy-3-methylbutyl]-7-methoxy-2H-1-benzopyran-2-one CAS 5875-49-0
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