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METHYL 4-AMINO-6-INDOLECARBOXYLATE

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Products Intro: Product Name:METHYL 4-AMINO-6-INDOLECARBOXYLATE
CAS:121561-15-7
Purity:0.99 Package:5KG;1KG
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CAS:121561-15-7
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CAS:121561-15-7
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CAS:121561-15-7
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METHYL 4-AMINO-6-INDOLECARBOXYLATE manufacturers

METHYL 4-AMINO-6-INDOLECARBOXYLATE Basic information
Product Name:METHYL 4-AMINO-6-INDOLECARBOXYLATE
Synonyms:Methyl 4-Amino-6-indolecarboxylate Hydrochloride;4-AMINO-6-METHOXYCARBONYL INDOLE;Methyl4-amino-1H-indole-6-carboxylate;4-amino-6-indole carboxylic acid methyl ester ,95%;4-amino-1H-indole-6-carboxylic acid methyl ester hydrochloride;1H-Indole-6-carboxylic acid, 4-aMino-, Methyl ester;4-AMino-6-Methylcarboxylateindole;Methyl 4-AMino-6-indolecarboxylate Hy
CAS:121561-15-7
MF:C10H10N2O2
MW:190.2
EINECS:
Product Categories:Acids and Derivatives;Heterocycles;Indole/indoline/oxindole;Indole;Heterocyclic Compounds;AMINOACID
Mol File:121561-15-7.mol
METHYL 4-AMINO-6-INDOLECARBOXYLATE Structure
METHYL 4-AMINO-6-INDOLECARBOXYLATE Chemical Properties
Melting point 160-163 °C(Solv: benzene (71-43-2))
Boiling point 429.8±25.0 °C(Predicted)
density 1.339±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka17.03±0.30(Predicted)
AppearanceLight brown to brown Solid
CAS DataBase Reference121561-15-7(CAS DataBase Reference)
Safety Information
MSDS Information
METHYL 4-AMINO-6-INDOLECARBOXYLATE Usage And Synthesis
UsesIn the pharmaceutical field, methyl 4-amino-6-indolecarboxylate is mainly used as an organic synthesis intermediate to synthesize a variety of drug compounds, such as methyl 4-amino-6-indolecarboxylate hydrochloride, which is used in drug synthesis.
Synthesis
(E)-Methyl 4-(2-(diMethylaMino)vinyl)-3,5-dinitrobenzoate

597562-13-5

METHYL 4-AMINO-6-INDOLECARBOXYLATE

121561-15-7

To a solution of methyl 4-[(E)-2-(dimethylamino)vinyl]-3,5-dinitrobenzoate (D200) (10 g, 34 mmol, 1 eq.) in methanol (250 ml) was added 10% palladium charcoal (50% wet, 1.0 g, 5% w/w). The reaction mixture was stirred under hydrogen atmosphere for 7 hours. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filtrate was concentrated under reduced pressure. The residue was ground with ethyl acetate/isohexane mixed solvent to afford methyl 4-amino-1H-indole-6-carboxylate (D201) (5 g, 77% yield) as a dark pink solid. Mass spectrometry analysis showed [M+H]+ = 191.0 and retention time (RT) = 1.20 min.

References[1] Tetrahedron Letters, 2007, vol. 48, # 45, p. 7990 - 7993
[2] Patent: WO2004/50619, 2004, A1. Location in patent: Page 57
[3] Patent: WO2005/58915, 2005, A1. Location in patent: Page/Page column 18
Tag:METHYL 4-AMINO-6-INDOLECARBOXYLATE(121561-15-7) Related Product Information
4-BENZYLOXY-6-INDOLE CARBOXYLIC ACID METHYL ESTER 4-HYDROXY-1H-INDOLE-6-CARBOXYLIC ACID METHYL ESTER 1H-Indole-6-carboxylic acid, 4-chloro-, Methyl ester 1H-Indole, 4-broMo-6-chloro- 1H-Indole-6-carboxylic acid, 4-fluoro-, Methyl ester METHYL 4-CHLORO-3-METHYLBENZOATE METHYL 4-[(4-METHYLPIPERAZIN-1-YL)METHYL]BENZOATE METHYL 4-(TRIFLUOROMETHYL)NICOTINATE METHYL 4-BROMO-2-BROMOMETHYL-BENZOATE 1H-Indole, 4-broMo-6-(phenylMethoxy)- 4-NITRO-6-INDOLECARBOXYLIC ACID METHYL ESTER METHYL 6-AMINO-4-INDOLECARBOXYLATE,Methyl 6-Amino-4-indolecarboxylate Hydrochloride Indole-6-carboxylic acid Methyl indole-6-carboxylate 6-HYDROXYMETHYLINDOLE Indole-6-carboxaldehyde 4-Aminoindole METHYL 4-AMINO-6-INDOLECARBOXYLATE

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