Phthalimide → HCID 67231570, compound

HRID 2035560Notes

Reaction equation

HRID 2035560 reaction equation
CCOC(/N=N/C(OCC)=O)=O.[Si:13]([O:20][C:21]1[CH:22]=[CH:23][CH:24]=[C:25]2[C:30]=1[N:29]=[C:28]([C:31]1[N:35]3[CH:36]=[CH:37][C:38]([CH2:40]O)=[CH:39][C:34]3=[N:33][N:32]=1)[CH:27]=[CH:26]2)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14].[C:42]1(=[O:52])[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[C:44](=[O:51])[NH:43]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1COCC1>[Si:13]([O:20][C:21]1[CH:22]=[CH:23][CH:24]=[C:25]2[C:30]=1[N:29]=[C:28]([C:31]1[N:35]3[CH:36]=[CH:37][C:38]([CH2:40][N:43]4[C:44](=[O:51])[C:45]5[C:50](=[CH:49][CH:48]=[CH:47][CH:46]=5)[C:42]4=[O:52])=[CH:39][C:34]3=[N:33][N:32]=1)[CH:27]=[CH:26]2)([C:16]([CH3:17])([CH3:18])[CH3:19])([CH3:14])[CH3:15]

Participants

6

Procedure

DEAD (0.6524 mL, 4.143 mmol) was added to a solution of (3-(8-(tert-butyldimethylsilyloxy)quinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)methanol (1.123 g, 2.762 mmol), isoindoline-1,3-dione (0.6096 g, 4.143 mmol) and triphenylphosphine (1.087 g, 4.143 mmol) in THF (20 mL) at 0° C. Following addition, the cold bath was removed and the reaction stirred at ambient temperature for 3 hours. The crude reaction was concentrated and the residue was purified by flash column chromatography (eluting with at 1:4 mixture of ethyl acetate/Hexanes) to afford the desired product mixed with triphenylphosphine oxide.

Workup

  1. additionaddition
  2. customthe cold bath was removed
  3. customThe crude reaction
  4. concentrationwas concentrated
  5. customthe residue was purified by flash column chromatography (eluting with at 1:4 mixture of ethyl acetate/Hexanes)

Sources & evidence

ORD record
ord-78b59663724a41f68e2e90e165cfeeb9
Source dataset
uspto-grants-2013_11
Patent number
US08575145B2

Reaction notes

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