Triethylamine → 2-[(2-Indolyl)carbonylamino]-5-methoxy-4-phenylthiazole

HRID 1769105Notes

Reaction equation

HRID 1769105 reaction equation
[NH2:1][C:2]1[S:3][C:4]([O:13][CH3:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.C([N:18]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[C:19]1[C:27](O)=[O:28])(=O)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.C(N(CC)CC)C>C(Cl)Cl.O>[NH:18]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[C:19]1[C:27]([NH:1][C:2]1[S:3][C:4]([O:13][CH3:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1)=[O:28]

Participants

7

Procedure

3.15 g of 2-amino-5-methoxy-4-phenylthiazole are dissolved in 60 ml of CH2Cl2. 3.26 g of 1-acetylindole-2-carboxylic acid, 8.12 g of BOP and 1.86 g of triethylamine are added, and the reaction mixture is stirred at room temperature for one week. 50 ml of water are added and the organic phase is decanted, dried over Na2SO4, filtered and concentrated under vacuum. The residue is taken up in 100 ml of methanol, and 10 g of K2CO3 are added and the mixture is stirred overnight at room temperature. The mixture is concentrated under vacuum, and the residue is taken up in water, and the precipitate formed is separated by filtration and washed with CH2Cl2.

Workup

  1. customthe organic phase is decanted
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated under vacuum
  5. addition10 g of K2CO3 are added
  6. stirringthe mixture is stirred overnight at room temperature
  7. concentrationThe mixture is concentrated under vacuum
  8. customthe precipitate formed
  9. customis separated by filtration
  10. washwashed with CH2Cl2

Sources & evidence

ORD record
ord-e12a4fe56acd4f7cba2026109b320220
Source dataset
uspto-grants-1995_01
Patent number
US05380736

Reaction notes

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