ChemicalBook--->CAS DataBase List--->28179-47-7

28179-47-7

28179-47-7 Structure

28179-47-7 Structure
IdentificationMore
[Name]

5-Aminoisophthalic acid monomethyl ester
[CAS]

28179-47-7
[Synonyms]

3-AMINO-5-(METHOXYCARBONYL)BENZOIC ACID
5-AMINOISOPHTHALIC ACID MONOMETHYL ESTER
CHEMPACIFIC 41247
Monomethyl 5-aminoisophthalate
5-AMINOISOPHTHALIC ACID MONOMETHYLESTER3-AMINO-5-(METHOXYCARBONYL)BENZOIC ACID
[Molecular Formula]

C9H9NO4
[MDL Number]

MFCD00224870
[Molecular Weight]

195.17
[MOL File]

28179-47-7.mol
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C(protect from light)
[Appearance]

Light yellow to yellow Solid
[CAS DataBase Reference]

28179-47-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2922290090
Spectrum DetailBack Directory
[Spectrum Detail]

5-Aminoisophthalic acid monomethyl ester(28179-47-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 5-nitroisophthalate

1955-46-0

5-Aminoisophthalic acid monomethyl ester

28179-47-7

Example 14: Synthesis of methyl 5-((1R,2S)-2-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidine-1-carbonyl)cyclohexylcarbamoyl)biphenyl-3-carboxylate Step 1: Preparation of 3-amino-5-(methoxycarbonyl)benzoic acid Under argon protection, 20% Pd(OH)2 (0.50 g) was carefully wetted with methanol (5 mL), followed by addition of a methanol (20 mL) solution of 3-(methoxycarbonyl)-5-nitrobenzoic acid (5.00 g, 22.2 mmol). The mixture was placed in a Parr shaker and hydrogenated under 50 psi hydrogen pressure for 5 hours. Upon completion of the reaction, the reaction mixture was carefully filtered through glass fiber filter paper under argon protection. The filtrate was concentrated to give the off-white solid product 3-amino-5-(methoxycarbonyl)benzoic acid (4.0 g, 20.5 mmol, 92% yield). Mass spectrometry analysis resulted in (M-H)+ = 194.

[References]

[1] Patent: WO2009/15166, 2009, A1. Location in patent: Page/Page column 87
[2] Chemical Communications, 2012, vol. 48, # 40, p. 4809 - 4811
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 10, p. 2654 - 2660
[4] Patent: US2007/32470, 2007, A1. Location in patent: Page/Page column 8-9
[5] Patent: US2006/223759, 2006, A1. Location in patent: Page/Page column 193
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