Triethylsilane → 3-[6-(3-Trifluoromethyl-benzyloxy)-pyridin-3-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

HRID 1024196Notes

Reaction equation

HRID 1024196 reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]([CH:10]([C:12]2[CH:13]=[N:14][C:15]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=3)=[CH:16][CH:17]=2)O)=[CH:2]1.C([SiH](CC)CC)C>FC(F)(F)C(O)=O.O>[F:28][C:26]([F:27])([F:29])[C:22]1[CH:21]=[C:20]([CH:25]=[CH:24][CH:23]=1)[CH2:19][O:18][C:15]1[N:14]=[CH:13][C:12]([CH2:10][C:3]2[C:4]3[C:5](=[N:6][CH:7]=[CH:8][CH:9]=3)[NH:1][CH:2]=2)=[CH:17][CH:16]=1

Participants

5

Procedure

(1H-Pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanol 74 was dissolved in 9:1 trifluoroacetic acid: triethylsilane. The reaction was stirred at room temperature for 15 hours. The reaction was diluted with water and extracted with ethyl acetate and concentrated. The crude material was purified by reverse phase HPLC to provide 3-[6-(3-Trifluoromethyl-benzyloxy)-pyridin-3-ylmethyl]-1H-pyrrolo[2,3-b]pyridine P-0057. MS (ESI) [M+H+]+=384.3.

Workup

  1. extractionextracted with ethyl acetate
  2. concentrationconcentrated
  3. customThe crude material was purified by reverse phase HPLC

Sources & evidence

ORD record
ord-0836b6cb946e4a65bb41fd4171dcd976
Source dataset
uspto-grants-2014_05
Patent number
US08722702B2

Reaction notes

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