Acetic Acid → Methyl alpha-Methyl-1-nitro-1,2-dihydro-6-azanaphthalene-2-acetate

HRID 1252583Notes

Reaction equation

HRID 1252583 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][N:8]=[CH:9]2)([O-:3])=[O:2].[C:14](#N)[CH3:15].CN([S+](N(C)C)N(C)C)C.[CH3:27][Si-](F)(F)(C)C.[C:33](O)(=[O:35])C.[OH2:37]>CCCCCC>[CH3:27][CH:14]([CH:13]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[N:8][CH:9]=2)[CH:4]1[N+:1]([O-:3])=[O:2])[C:15]([O:35][CH3:33])=[O:37]

Participants

7

Reactant 5

HCID 176Acetic AcidHCID 962WaterHCID 6342AcetonitrileHCID 690855-NitroisoquinolineHCID 9795567Tris(dimethylamino)sulfonium difluorotrimethylsilicate

Product 1

HCID 13507926Methyl alpha-Methyl-1-nitro-1,2-dihydro-6-azanaphthalene-2-acetate

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

A flame dried 50 mL flask fitted with an addition funnel was charged with 0.872 g (500 mmol) of 5-nitroisoquinoline and 0.95 mL (5.1 mmol) of MTS. An acetonitrile solution of 1.40 g (5.09 mmol) of TASF was slowly added to the reaction mixture in 15 min at -78° C. The mixture was stirred for 22 h at that temperature. One mL of acetic acid in 5 mL of hexane was added, and reaction was warmed to room temperature. After 30 min, 40 mL of water was added. The solid which precipitated out was collected and analyzed. The product yield was 0.972 g (74%). The product material was analyzed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.

Workup

  1. customA flame dried 50 mL flask
  2. customfitted with an addition funnel
  3. customreaction
  4. waitAfter 30 min
  5. customThe solid which precipitated out
  6. customwas collected

Sources & evidence

ORD record
ord-2d0df3e441734288804ff2deaa44fdf9
Source dataset
uspto-grants-1988_05
Patent number
US04743690

Reaction notes

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