Water → HCID 59589532, compound

HRID 1472850Notes

Reaction equation

HRID 1472850 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17]2[N:22]3[N:23]=[C:24]([NH:26][C:27]4[CH:32]=[CH:31][C:30]([O:33][CH2:34][CH2:35][N:36]5[CH2:40][CH2:39][CH2:38][CH2:37]5)=[CH:29][CH:28]=4)[N:25]=[C:21]3[CH:20]=[CH:19][CH:18]=2)[CH:12]=1)C.O>C(OCC)C>[N:36]1([CH2:35][CH2:34][O:33][C:30]2[CH:29]=[CH:28][C:27]([NH:26][C:24]3[N:25]=[C:21]4[CH:20]=[CH:19][CH:18]=[C:17]([C:13]5[CH:12]=[C:11]([CH2:10][OH:9])[CH:16]=[CH:15][CH:14]=5)[N:22]4[N:23]=3)=[CH:32][CH:31]=2)[CH2:40][CH2:39][CH2:38][CH2:37]1

Participants

5

Procedure

To a slurry of lithium aluminium hydride (82.6 mg, 2.12 mmol) in diethylether (10 mL) was added 3-{2-[4-(2-pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzoic acid ethyl ester (0.50 g, 1.06 mmol) portionwise. The mixture was stirred at room temperature for 6 hrs. Water was added to quench the hydride and the aqueous layer was removed. The organic layer was concentrated in vacuo, and the crude product loaded onto an SCX column, which was washed with methanol and the product eluted with 2M ammonia in methanol, then concentrated in vacuo. Yield: 0.35 g, 76%. A small amount was purified by preparatory HPLC. RT: 2.32, MI: 430, Method: 2.

Workup

  1. customto quench the hydride
  2. customthe aqueous layer was removed
  3. concentrationThe organic layer was concentrated in vacuo
  4. washwas washed with methanol
  5. washthe product eluted with 2M ammonia in methanol
  6. concentrationconcentrated in vacuo
  7. customA small amount was purified by preparatory HPLC
  8. customRT

Sources & evidence

ORD record
ord-d827082d3e304db0a8ee36a492bb12dc
Source dataset
uspto-grants-2015_04
Patent number
US09012633B2

Reaction notes

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