ChemicalBook--->CAS DataBase List--->1092351-82-0

1092351-82-0

1092351-82-0 Structure

1092351-82-0 Structure
IdentificationBack Directory
[Name]

Methyl 1-methyl-indazole-5-carboxylate
[CAS]

1092351-82-0
[Synonyms]

Methyl 1-methyl-indazole-5-carboxylate
1-METHYL-1H-INDAZOLE-5-CARBOXYLIC ACID M
5-(Methoxycarbonyl)-1-methyl-1H-indazole
Methyl 1-Methyl-1H-indazol-5-carboxylate
methyl 1-methyl-1H-indazole-5-carboxylate
1-Methyl-1H-indazole-5-carboxylic acid methyl ester
1H-Indazole-5-carboxylic acid, 1-methyl-, methyl ester
1-METHYL-1H-INDAZOLE-5-CARBOXYLIC ACID METHYL ESTER(WX618113)
[Molecular Formula]

C10H10N2O2
[MDL Number]

MFCD11109401
[MOL File]

1092351-82-0.mol
[Molecular Weight]

190.199
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 1-methyl-indazole-5-carboxylate(1092351-82-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 1H-indazole-5-carboxylate

473416-12-5

Iodomethane

74-88-4

Methyl 1-methyl-indazole-5-carboxylate

1092351-82-0

Methyl 1H-indazole-5-carboxylate (22 g, 0.13 mol) and iodomethane (62 g, 0.44 mol) were added to potassium carbonate (60 g, 0.44 mol) in N,N-dimethylformamide (200 mL). Subsequently, iodomethane was added dropwise at room temperature and the reaction mixture was stirred for 5 hours. Upon completion of the reaction, the reaction was quenched by the addition of water (200 mL) and extracted with ethyl acetate (4 x 200 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. Purification by silica gel column chromatography using a petroleum ether solution containing 2% ethyl acetate as eluent gave methyl 1-methyl-1H-indazole-5-carboxylate as an orange solid (13 g, 55% yield). The product was analyzed by LC-MS (ES, m/z): [M + H]+ 191.0. 1H NMR (300 MHz, DMSO-d6) δ: 8.48 (s, 1H), 8.24 (s, 1H), 7.97-7.94 (dd, J = 1.50, 8.70 Hz, 1H), 7.77-7.72 (m, 1H), 4.09 (s. 3H), 3.88 (s, 3H).

[References]

[1] Journal of Organic Chemistry, 2014, vol. 79, # 16, p. 7286 - 7293
[2] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[3] Patent: WO2009/144554, 2009, A1. Location in patent: Page/Page column 48
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