Sodium Carbonate → 5-(2-Thiophen-2-yl-phenyl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine

HRID 1877958Notes

Reaction equation

HRID 1877958 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[N:13]2[CH:14]=[N:15][CH:16]=[C:12]2[CH2:11][CH2:10][CH2:9]1.[S:17]1[CH:21]=[CH:20][CH:19]=[C:18]1B(O)O.C([O-])([O-])=O.[Na+].[Na+]>COCCOC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[S:17]1[CH:21]=[CH:20][CH:19]=[C:18]1[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[N:13]2[CH:14]=[N:15][CH:16]=[C:12]2[CH2:11][CH2:10][CH2:9]1

Participants

6

Procedure

To a solution of 5-(2-bromophenyl)-5,6,7,8,-tetrahydro-imidazo[1,5-a]pyridine, Example 12D (120 mg, 0.43 mmol) in DME (2 mL) is added thiophene-2-boronic acid (166 mg, 1.3 mmol), aqueous Na2CO3 (2M, 1.0 mL, 2.0 mmol), and Pd(PPh3)4 (20 mg). The reaction mixture is refluxed overnight. The mixture is partitioned between EtOAc and 1M NaOH. The organic layer is washed by sat. NaHCO3, dried and concentrated to give an oil. The crude reaction mixture is subjected to flash chromatography (silica gel) eluting with acetone:hexane to yield the desired compound. MS (ESI) m/z 280 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.58-1.74 (m, 1 H), 1.85-2.01 (m, 2 H), 2.14-2.27 (m, 1 H), 2.74-2.94 (m, 2 H), 5.45 (dd, J=8.6, 5.1 Hz, 1 H), 6.81 (s, 1 H), 7.00-7.05 (m, 2 H), 7.06 (s, 1 H), 7.10 (dd, J=5.3, 3.5 Hz, 1 H), 7.31-7.37 (m, 2 H), 7.39 (dd, J=5.2, 1.1 Hz, 1 H), 7.41-7.46 (m, 1 H).

Workup

  1. temperatureThe reaction mixture is refluxed overnight
  2. customThe mixture is partitioned between EtOAc and 1M NaOH
  3. washThe organic layer is washed by sat. NaHCO3
  4. customdried
  5. concentrationconcentrated
  6. customto give an oil
  7. customThe crude reaction mixture
  8. washeluting with acetone

Sources & evidence

ORD record
ord-80a219c113a84b77ba7af52c6e9341dc
Source dataset
uspto-grants-2012_11
Patent number
US08314097B2

Reaction notes

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