Citric Acid → HCID 71187264, compound

HRID 1529254Notes

Reaction equation

HRID 1529254 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 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-09894de4ff7f423b9056c3e53b13febb
Source dataset
uspto-grants-2015_07
Patent number
US09090614B2

Reaction notes

Loading…