Pyridine → HCID 57855892, compound

HRID 2039637Notes

Reaction equation

HRID 2039637 reaction equation
[NH2:1][C:2]1[C:3]([CH3:19])=[C:4]2[C:9](=[CH:10][C:11]=1[C:12]([OH:14])=[O:13])[N:8]=[C:7]([C:15]([F:18])([F:17])[F:16])[CH:6]=[CH:5]2.[Cl:20][C:21]1[C:22]([N:27]2[C:31]([C:32](O)=O)=[CH:30][C:29]([C:35]([F:38])([F:37])[F:36])=[N:28]2)=[N:23][CH:24]=[CH:25][CH:26]=1.N1C=CC=CC=1.CS(Cl)(=O)=O>C(#N)C.C(OCC)(=O)C.CCCCCC>[Cl:20][C:21]1[C:22]([N:27]2[C:31]([C:32]3[O:13][C:12](=[O:14])[C:11]4[C:2](=[C:3]([CH3:19])[C:4]5[C:9]([CH:10]=4)=[N:8][C:7]([C:15]([F:18])([F:16])[F:17])=[CH:6][CH:5]=5)[N:1]=3)=[CH:30][C:29]([C:35]([F:38])([F:36])[F:37])=[N:28]2)=[N:23][CH:24]=[CH:25][CH:26]=1

Participants

8

Procedure

A solution of 6-Amino-5-methyl-2-trifluoromethyl-quinoline-7-carboxylic acid (0.60 g, 2.22 mmol), 2-(3-Chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (0.65 g 2.22 mmol) and pyridine (0.79 g, 9.992 mmol) in acetonitrile (30 ml) is cooled to 0-5° C. and treated drop wise with methane sulphonyl chloride (0.89 g, 7.77 mmol) dissolved in ca. 2 ml of acetonitrile. TLC analysis (4:1 hexane:ethyl acetate) after 2 hr shows reaction completion. The reaction mixture is concentrated to ca. 2/3 the original volume in vacuo and then poured onto 75 ml of ice/water. The resultant crystals are filtered at the pump, washed with water and dried in vacuo. This gives the title compound (1.0 g, 85.7%) as orange crystals.

Workup

  1. customreaction completion
  2. concentrationThe reaction mixture is concentrated to ca. 2/3 the original volume in vacuo
  3. additionpoured onto 75 ml of ice/water
  4. filtrationThe resultant crystals are filtered at the pump
  5. washwashed with water
  6. customdried in vacuo

Sources & evidence

ORD record
ord-0be1f2a682474eb29340a7d9680df7d9
Source dataset
uspto-grants-2013_11
Patent number
US08580785B2

Reaction notes

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