Methanol → 1-(4-Methylpyridin-3-yl)-3-(4-methylthieno[3,2-e]pyridin-2-yl)imidazolidin-2-one

HRID 80203

Reaction equation

HRID 80203 reaction equation
[C:1](=O)([O-])[O-].[K+].[K+].Cl[C:8]1[C:13]2[CH:14]=[C:15]([N:17]3[CH2:21][CH2:20][N:19]([C:22]4[CH:23]=[N:24][CH:25]=[CH:26][C:27]=4[CH3:28])[C:18]3=[O:29])[S:16][C:12]=2[CH:11]=[CH:10][N:9]=1.CB(O)O.CO>C(Cl)(Cl)Cl.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:28][C:27]1[CH:26]=[CH:25][N:24]=[CH:23][C:22]=1[N:19]1[CH2:20][CH2:21][N:17]([C:15]2[S:16][C:8]3[N:9]=[CH:10][CH:11]=[C:12]([CH3:1])[C:13]=3[CH:14]=2)[C:18]1=[O:29]

Participants

7

Reactant 4

HCID 887MethanolHCID 11430Potassium CarbonateHCID 139377Methylboronic AcidHCID 498718701-(4-Chloro-thieno[3,2-c]pyridin-2-yl)-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

Product 1

HCID 687826491-(4-Methylpyridin-3-yl)-3-(4-methylthieno[3,2-e]pyridin-2-yl)imidazolidin-2-oneYield 16.39%

Reagents, catalysts & solvents 2

HCID 11979704Tetrakis(triphenylphosphine)palladiumCatalystHCID 6212ChloroformSolvent

Procedure

Tetrakis (triphenylphosphine) palladium (33 mg, 0.0288 mmol) was added to potassium carbonate (120 mg, 0.8649 mmol) previously purged with argon (30 minutes). The reaction mixture was purged with argon for 15 minutes, followed by the addition of 1-(4-chloro-thieno[3,2-c]pyridin-2-yl)-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (98A: 100 mg, 0.2883 mmol) and methyl boronic acid (21 mg, 0.3459 mmol). The reaction mixture was heated to reflux for 6 hours. The reaction was monitored by TLC (10% MeOH in CHCl3). The reaction mixture was concentrated to afford the crude product. Purification by column chromatography on silica gel (3-4% MeOH in CHCl3), followed by preparative HPLC afforded 10 mg of the product (16.39% yield).

Workup

  1. custompreviously purged with argon (30 minutes)
  2. customThe reaction mixture was purged with argon for 15 minutes
  3. temperatureThe reaction mixture was heated
  4. temperatureto reflux for 6 hours
  5. concentrationThe reaction mixture was concentrated
  6. customto afford the crude product
  7. customPurification by column chromatography on silica gel (3-4% MeOH in CHCl3)

Sources & evidence

ORD record
ord-d1ef7f24fe0c4034b7ba44cc299852fa
Source dataset
uspto-grants-2014_09
Patent number
USRE045173E1

Linked notes

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