Water → HCID 86630675, compound

HRID 1915565Notes

Reaction equation

HRID 1915565 reaction equation
Cl.[C:2]1([C:8]2[C:9]([C:17]3[CH:22]=[CH:21][C:20]([CH2:23]N4CCC(C5N=C(C6C=CC=CN=6)NN=5)CC4)=[CH:19][CH:18]=3)=[N:10][C:11]3[N:12]([N:14]=[CH:15][CH:16]=3)[CH:13]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:41]N1C(=O)CCC1=O.[OH2:49]>C(Cl)(Cl)Cl.ClCCl>[Br:41][C:16]1[CH:15]=[N:14][N:12]2[CH:13]=[C:8]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C:9]([C:17]3[CH:22]=[CH:21][C:20]([CH:23]=[O:49])=[CH:19][CH:18]=3)=[N:10][C:11]=12

Participants

6

Procedure

1.0 g 6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde (prepared as described under example 19) and 0.65 g N-bromosuccinimide are refluxed in 30 ml Chloroform for 5 h. This mixture is worked up by diluting with water and extraction with dichloromethane. The organic layers are dried over Na2SO4 and concentrated to yield the crude product, which is suspended in ethyl acetate/petrol ether. The solid desired product is isolated by filtration.

Workup

  1. dry with materialThe organic layers are dried over Na2SO4
  2. concentrationconcentrated
  3. customto yield the crude product, which

Sources & evidence

ORD record
ord-fcee1c75b0164b6180eeeceb21748448
Source dataset
uspto-grants-2013_12
Patent number
US08614218B2

Reaction notes

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