Ethyl orthoformate → HCID 13385681, compound

HRID 2412872Notes

Reaction equation

HRID 2412872 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH:12][NH2:13])[C:6]([O:14][CH3:15])=[N:5]2.[CH:16](OCC)(OCC)OCC>>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[CH:16]=[N:13][N:12]=[C:7]1[C:6]([O:14][CH3:15])=[N:5]2

Participants

3

Reactant 2

HCID 31214Ethyl orthoformateHCID 13385671HCID 13385671, compound

Product 1

HCID 13385681HCID 13385681, compound

Conditions

Temperature
100 °C

Procedure

A mixture consisting of 15 g. (0.072 mole) of 6-fluoro-2-hydrazino-3-methoxyquinoxaline and 250 ml. of triethyl orthoformate was heated with mechanical stirring in a preheated oil both at 100° C. overnight (~16 hours). The resulting mixture was then cooled to room temperature, and the precipitate which formed was subsequently recovered by means of suction filtration and washed with ethanol to ultimately afford 11.3 g (72%) of pure 7-fluoro-4-methoxy-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 245°-246° C. (decomp.).

Workup

  1. temperatureThe resulting mixture was then cooled to room temperature
  2. customthe precipitate which formed
  3. filtrationwas subsequently recovered by means of suction filtration
  4. washwashed with ethanol to ultimately afford 11.3 g (72%) of pure 7-fluoro-4-methoxy-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 245°-246° C. (decomp.)

Sources & evidence

ORD record
ord-9c66af2fa4f54313b207399d2a9fd7ad
Source dataset
uspto-grants-1985_01
Patent number
US04495187

Reaction notes

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