1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE

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Products Intro: Product Name:N-Methoxy-N-methyl-1H-indazole-3-carboxamide
CAS:351457-12-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-55791
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Products Intro: Product Name:N-Methoxy-N-methyl-1H-indazole-3-carboxamide
CAS:351457-12-0
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Products Intro: Product Name:1H-Indazole-3-carboxamide, N-methoxy-N-methyl-
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Products Intro: Product Name:1H-Indazole-3-carboxamide, N-methoxy-N-methyl-
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Products Intro: Product Name:1H-Indazole-3-carboxamide, N-methoxy-N-methyl-
CAS:351457-12-0
Purity:99 Package:5KG;1KG,25kg
1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE Basic information
Product Name:1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE
Synonyms:1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE;1H-Indazole-3-carboxamide, N-methoxy-N-methyl-;N-Methoxy-N-Methyl-1H-indazole-3-carboxaMide;1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMID
CAS:351457-12-0
MF:C10H11N3O2
MW:205.21
EINECS:604-604-1
Product Categories:
Mol File:351457-12-0.mol
1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE Structure
1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE Chemical Properties
storage temp. Store at room temperature
AppearanceWhite to yellow Solid
Safety Information
MSDS Information
1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE Usage And Synthesis
Synthesis
N,O-Dimethylhydroxylamine hydrochloride

6638-79-5

Indazole-3-carboxylic acid

4498-67-3

1H-INDAZOLE-3-(N-METHOXY-METHYL)CARBAMIDE

351457-12-0

Indazole-3-carboxylic acid (10 g, 61.7 mmol) was used as a raw material, which was dissolved in DMF (100 mL), and carbonyldiimidazole (11 g, 67.84 mmol) was slowly added at room temperature, and gas was observed to be released during the reaction for 15 min. Subsequently, the reaction mixture was heated to 65 °C and maintained for 2 hours. After completion of the reaction, the mixture was cooled to room temperature, N,O-dimethylhydroxylamine hydrochloride (4.14 g, 67.8 mmol) was added and the mixture was again heated to 65 °C and reacted overnight. At the end of the reaction, the reaction mixture was cooled, the reaction was quenched with water, extracted with dichloromethane (CH2Cl2) and the organic phase was washed with water. The organic phases were combined and concentrated after drying to afford the target product N-methoxy-N-methyl-1H-indazole-3-carboxamide (10.3 g, 81.4% yield).

References[1] Tetrahedron Letters, 2007, vol. 48, # 14, p. 2457 - 2460
[2] Tetrahedron, 2007, vol. 63, # 2, p. 419 - 428
[3] Patent: WO2008/71451, 2008, A1. Location in patent: Page/Page column 50
[4] Patent: WO2013/40215, 2013, A1. Location in patent: Paragraph 00334
[5] Patent: US2013/267495, 2013, A1. Location in patent: Paragraph 0409
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