Cesium carbonate → HCID 59216385, compound

HRID 2245715Notes

Reaction equation

HRID 2245715 reaction equation
[CH3:1][C:2]([C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[C:12](=[O:16])[NH:11][CH2:10][CH2:9]2)([CH3:5])[C:3]#[N:4].[Br:17][C:18]1[CH:25]=[CH:24][CH:23]=[C:22](Br)[C:19]=1[CH:20]=[O:21].C(=O)([O-])[O-].[Cs+].[Cs+]>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2>[Br:17][C:18]1[C:19]([CH:20]=[O:21])=[C:22]([N:11]2[CH2:10][CH2:9][C:8]3[C:13](=[CH:14][CH:15]=[C:6]([C:2]([CH3:1])([CH3:5])[C:3]#[N:4])[CH:7]=3)[C:12]2=[O:16])[CH:23]=[CH:24][CH:25]=1

Participants

6

Conditions

Temperature
110 °C

Procedure

To 1.3 g (6.07 mmol) 2-methyl-2-(1-oxo-1,2,3,4-tetrahydroisoquinolin-6-yl)-propionitrile dissolved in 20 ml degassed dioxane was added 6.40 g (24.27 mmol) 2,6-dibromobenzaldehyde, 3.96 g (12.14 mmol) cesium carbonate, 70 mg (0.121 mmol) Pd(dba)2, and 105 mg (0.182 mmol) xantphos. The mixture was heated to 110° C. for 3 h, cooled to room temperature, and filtered over Celite rinsing with dioxane. The mixture was then concentrated and purified by column chromatography, eluting with ethyl acetate/hexanes to provide 1.10 g (46%) 2-[2-(3-bromo-2-formylphenyl)-1-oxo-1,2,3,4-tetrahydroisoquinolin-6-yl]-2-methylpropionitrile.

Workup

  1. customdegassed dioxane
  2. temperaturecooled to room temperature
  3. filtrationfiltered over Celite
  4. washrinsing with dioxane
  5. concentrationThe mixture was then concentrated
  6. custompurified by column chromatography
  7. washeluting with ethyl acetate/hexanes

Sources & evidence

ORD record
ord-6180b5324b7a4792a71d6fb6cb33f380
Source dataset
uspto-grants-2010_03
Patent number
US07683064B2

Reaction notes

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