Ethanol → HCID 86744472, compound

HRID 1654065Notes

Reaction equation

HRID 1654065 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][N+:7]([O-])=[CH:6][C:5]=1F)([O-:3])=[O:2].[NH2:12][C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([CH3:22])=[CH:16]2.C([OH:25])C>>[N+:1]([C:4]1[CH:9]=[CH:8][N:7]=[CH:6][C:5]=1[NH+:12]([O-:25])[C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([CH3:22])=[CH:16]2)([O-:3])=[O:2]

Participants

4

Reactant 3

HCID 702EthanolHCID 5940283-Fluoro-4-nitropyridin-1-ium-1-olateHCID 27339925-Amino-2-methylindole

Product 1

HCID 86744472HCID 86744472, compound

Conditions

Temperature
50 °C

Procedure

A mixture of 4-nitro-3-fluoropyridine N-oxide (5.4 g) and 5-amino-2-methylindole (5.0 g) in 100 mL of thoroughly degassed absolute ethanol was stirred at 50° C. for 30 minutes and then cooled slowly to 0° C. The precipitate was collected and air dried to give 8.2 g of N-(4-nitro-3-pyridinyl)-2-methyl-1H-indol-5-amine N5 -oxide as a powder. This powder was taken up in 255 mL of absolute ethanol and hydrogenated at room temperature over 3% platinum on carbon at 50 psi. Filtration and concentration left 6.4 g of a solid which was purified by HPLC (7:3 dichloromethane/methanol) to give 3.0 g of a powder which was recrystallized from methanol/ether to give 1.8 g of crystals, m.p. 178-180 (with gas evolution).

Workup

  1. temperaturecooled slowly to 0° C
  2. customThe precipitate was collected
  3. customair dried

Sources & evidence

ORD record
ord-4cce9f34ddcc4b6ab2d573ec8eeb1db6
Source dataset
uspto-grants-1995_04
Patent number
US05405856

Reaction notes

Loading…