Citric Acid → HCID 71187264, compound

HRID 1844385Notes

Reaction equation

HRID 1844385 reaction equation
O.[OH-].[Li+].C1COCC1.[CH3:9][C:10]([NH:16][C:17]1[CH:22]=[CH:21][N:20]=[C:19]([C:23]2[C:31]3[C:26](=[N:27][CH:28]=[CH:29][CH:30]=3)[N:25](S(C3C=CC(C)=CC=3)(=O)=O)[CH:24]=2)[N:18]=1)([CH2:14][CH3:15])[C:11]([O-:13])=[O:12].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>O>[NH:25]1[C:26]2=[N:27][CH:28]=[CH:29][CH:30]=[C:31]2[C:23]([C:19]2[N:18]=[C:17]([NH:16][C:10]([CH3:9])([CH2:14][CH3:15])[C:11]([OH:13])=[O:12])[CH:22]=[CH:21][N:20]=2)=[CH:24]1

Participants

6

Procedure

Lithium hydroxide hydrate (1.9 g, 45 mmol) was added to 50 mL THF and 15 mL water. Then 2-methyl-2-((2-(1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)butanoate was added and the mixture was heated to reflux for 18 hours. The reaction was cooled to rt and 50 mL 1M citric acid solution was added. The mixture was extracted with 3×100 mL ethyl acetate where upon a white precipitate formed in the aqueous layer. The product was then filtered from the aqueous layer and dried under vacuum affording 1.6 g (68%) 2-((2-(1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)-2-methylbutanoic acid as white solid. 1H NMR (300 MHz, MeOD) 8.87 (dd, 1H), 8.32 (m, 2H), 7.94 (d, 1H), 3.31 (m, 3H), 2.80 (q, 1H), 2.29-1.95 (m, 2H), 1.68 (s, 3H), 0.96 (t, 3H). m/e m+1=312.22.

Workup

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 18 hours
  3. extractionThe mixture was extracted with 3×100 mL ethyl acetate where upon a white precipitate
  4. customformed in the aqueous layer
  5. filtrationThe product was then filtered from the aqueous layer
  6. customdried under vacuum

Sources & evidence

ORD record
ord-cae78353da9f4ca0abfc3e524b171050
Source dataset
uspto-grants-2015_02
Patent number
US08946425B2

Reaction notes

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