Acetyl chloride → N-[(cis)-1-acetyl-4-ethoxypyrrolidin-3-yl]-5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-amine

HRID 1824189Notes

Reaction equation

HRID 1824189 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:10]=[C:11]([CH2:26][CH3:27])[C:12]([NH:17][C@H:18]2[C@@H:22]([O:23][CH2:24][CH3:25])[CH2:21][NH:20][CH2:19]2)=[N:13][C:14]=1[CH2:15][CH3:16].[C:28](Cl)(=[O:30])[CH3:29].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[C:28]([N:20]1[CH2:21][C@H:22]([O:23][CH2:24][CH3:25])[C@H:18]([NH:17][C:12]2[C:11]([CH2:26][CH3:27])=[N:10][C:9]([C:3]3[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=3[Cl:1])=[C:14]([CH2:15][CH3:16])[N:13]=2)[CH2:19]1)(=[O:30])[CH3:29]

Participants

5

Procedure

To a solution of 5-(2,4-dichlorophenyl)-N-[(cis)-4-ethoxypyrrolidin-3-yl]-3,6-diethylpyrazin-2-amine (105 mg) in methylene chloride (5 ml) under N2 was added acetyl chloride (0.027 ml). The reaction mixture stirred for 30 min and was poured into saturated sodium bicarbonate (20 ml), extracted methylene chloride (2×20 ml), dried MgSO4, filtered and concentrated. MPLC chromatography was run on a biotage 25 S column with 60% ethyl acetate/heptane to provide the title compound as an oil (79 mg, 69%): 1H NMR (400 MHz, CDCl3) δ) 7.50, 7.34–7.26, 5.30, 5.12, 4.81, 4.19, 4.01, 3.87–3.67, 3.61–3.37, 2.72, 2.48, 1.33–1.26, 1.14; HRMS (FAB) calcd for C22H28Cl2N4O2+H 451.1667, found 451.1667.

Workup

  1. extractionextracted methylene chloride (2×20 ml), dried MgSO4
  2. filtrationfiltered
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-edd80b38f31048d0ba74f3ac82f89c07
Source dataset
uspto-grants-2006_05
Patent number
US07041672B2

Reaction notes

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