Iodoethane → HCID 70807095, compound

HRID 1631618Notes

Reaction equation

HRID 1631618 reaction equation
[N:1]1([C:7]2[N:8]=[C:9]([CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[NH:10][C:11](=[O:13])[CH:12]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH2:20](I)[CH3:21].C(=O)([O-])[O-].[Cs+].[Cs+]>>[CH2:20]([N:10]1[C:11](=[O:13])[CH:12]=[C:7]([N:1]2[CH2:2][CH2:3][O:4][CH2:5][CH2:6]2)[N:8]=[C:9]1[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH3:21]

Participants

4

Reactant 3

HCID 6340IodoethaneHCID 10796Cesium carbonateHCID 135905419Ethyl 2-[4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetate

Product 1

HCID 70807095HCID 70807095, compound

Procedure

The product is prepared according to the procedure described in example 67, using 600 mg of ethyl [4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetate prepared in stage 1 of example 1 and 0.23 ml of ethyl iodide in place of the methyl iodide, and replacing the potassium carbonate with cesium carbonate. After purification by silica column chromatography, eluent: 96/02/02 CH2Cl2/CH3CN/MeOH, 190 mg of ethyl [1-ethyl-4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetate are obtained in the form of a white solid the characteristics of which are the following:

Workup

  1. customThe product is prepared
  2. customAfter purification by silica column chromatography, eluent

Sources & evidence

ORD record
ord-b8895f27417d430c9892b4e70926410a
Source dataset
uspto-grants-2014_07
Patent number
US08791255B2

Reaction notes

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