HCID 136013917, compound → HCID 136121403, compound

HRID 2406159Notes

Reaction equation

HRID 2406159 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:9]1[N:18]=[C:17]([N:19]2[CH2:23][CH2:22][C@@H:21]([NH:24]C(=O)OCC3C=CC=CC=3)[CH2:20]2)[C:16]2[C:11](=[CH:12][C:13]([CH3:35])=[CH:14][CH:15]=2)[N:10]=1>CO.[Pd]>[NH2:24][C@@H:21]1[CH2:22][CH2:23][N:19]([C:17]2[C:16]3[C:11](=[CH:12][C:13]([CH3:35])=[CH:14][CH:15]=3)[N:10]=[C:9]([C:3]3[C:2]([F:1])=[CH:7][CH:6]=[CH:5][C:4]=3[OH:8])[N:18]=2)[CH2:20]1

Participants

4

Reactant 1

HCID 136013917HCID 136013917, compound

Product 1

HCID 136121403HCID 136121403, compoundYield 93.2%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

Under an N2 atmosphere, Pd/C (10% weight, 210 mg) was added to a solution of (R)-benzyl 1-(2-(2-fluoro-6-hydroxyphenyl)-7-methylquinazolin-4-yl)pyrrolidin-3-ylcarbamate (2.1 g, 4.44 mmol) in MeOH (60 mL). After purging 2 times with N2 and evacuating the atmosphere in the flask containing the reaction mixture, the reaction was stirred under an H2 atmosphere for 16 h. Since the reaction was not complete, an additional 200 mg Pd/C was added, and the reaction was stirred for an additional 4 h. The mixture was filtered through a pad of Celite (150 mL) using 1.8 mL MeOH, and the filtrate was concentrated under reduced pressure to obtain (R)-2-(4-(3-aminopyrrolidin-1-yl)-7-methylquinazolin-2-yl)-3-fluorophenol as a yellow solid (1.4 g, 93%). LC/MS: m/z 339.1 (M+H)+ at 1.05 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Workup

  1. customAfter purging 2 times with N2
  2. customevacuating the atmosphere in the flask
  3. additioncontaining the reaction mixture
  4. additionan additional 200 mg Pd/C was added
  5. stirringthe reaction was stirred for an additional 4 h
  6. filtrationThe mixture was filtered through a pad of Celite (150 mL)
  7. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-7d6a85e9df754583b392ea53bf84b10d
Source dataset
uspto-grants-2014_08
Patent number
US08809353B2

Reaction notes

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