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6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine → 6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine

HRID 73703
Notes
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Reaction equation

HRID 73703 reaction equation
Br[C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH2:11].[CH3:12][Zn]C>O1CCOCC1>[CH3:12][C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH2:11]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 579552016-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 178477796HCID 178477796, compound

Product 1

HCID 552886216-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineYield 79.8%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Conditions

Temperature
90 °C

Procedure

To a degassed solution of 6-bromopyrrolo[2,1-f][1,2,4]triazin-4-amine (Intermediate AAE) (316 mg, 1.48 mmol) and Bis(diphenylphosphino)ferrocenepalladium dichloride (30 mg, 0.037 mmol) in 1,4-dioxane (10 mL), was added dimethyl zinc (2.97 mL, 5.93 mmol, 2.0 M in toluene). The mixture was allowed to stir at 90° C. for 17 hr and then cooled to 0° C. The reaction was quenched with MeOH (1.0 mL) and partitioned between ethyl acetate (200 mL) and potassium phosphate dibasic pH 10 buffer (100 mL). The layers were separated and the organic phase was washed with brine, dried (Na2SO4), and concentrated to dryness. Trituration with Et2O afforded 175 mg (79%) of the desired product. 1H-NMR (DMSO-d6) δ 7.69 (s, 1H), 7.39 (s, 1H), 6.61 (s, 1H), 2.18 (s, 3H); MS [M+H]+=148.9; LCMS RT=1.16.

Workup

  1. temperaturecooled to 0° C
  2. customThe reaction was quenched with MeOH (1.0 mL)
  3. custompartitioned between ethyl acetate (200 mL) and potassium phosphate dibasic pH 10 buffer (100 mL)
  4. customThe layers were separated
  5. washthe organic phase was washed with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated to dryness

Sources & evidence

ORD record
ord-784f3fdca21a43168e8721118d5b2880
Source dataset
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08829185B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes