HCID 86629757, compound → HCID 59382684, compound

HRID 2354858Notes

Reaction equation

HRID 2354858 reaction equation
FC(F)(F)C(O)=O.[C:8]([C:10]1[CH:11]=[C:12]([NH:16][C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[C:24]([NH:27][C:28](=[O:36])[CH:29]=[C:30]4[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]4)[CH:25]=3)[N:20]=[CH:19][N:18]=2)[CH:13]=[CH:14][CH:15]=1)#[CH:9]>C(OCC)(=O)C>[C:8]([C:10]1[CH:11]=[C:12]([NH:16][C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[C:24]([NH:27][C:28](=[O:36])[CH:29]=[C:30]4[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]4)[CH:25]=3)[N:20]=[CH:19][N:18]=2)[CH:13]=[CH:14][CH:15]=1)#[CH:9]

Participants

3

Procedure

N-(4-(3-ethynylphenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate was dissolved in ethyl acetate. The mixture was washed once with saturated Na2CO3 and once with brine, dried over anhydrous magnesium sulfate, filtered, and evaporated in vacuo to give the title product. MS (EI) 384 (M+1).

Workup

  1. washThe mixture was washed once with saturated Na2CO3 and once with brine
  2. dry with materialdried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. customevaporated in vacuo

Sources & evidence

ORD record
ord-b5f6182e803d4a4cac2ba7b930088c37
Source dataset
uspto-grants-2010_07
Patent number
US07754729B2

Reaction notes

Loading…