HCID 136238744, compound → HCID 136378672, compound

HRID 2278555Notes

Reaction equation

HRID 2278555 reaction equation
C([O:3][C:4](=[O:20])[CH2:5][C:6]1[NH:7][C:8](=[O:19])[CH:9]=[C:10]([N:12]2[CH2:17][CH2:16][O:15][CH:14]([CH3:18])[CH2:13]2)[N:11]=1)C>CS(C)=O>[CH3:18][CH:14]1[O:15][CH2:16][CH2:17][N:12]([C:10]2[N:11]=[C:6]([CH2:5][C:4]([OH:20])=[O:3])[NH:7][C:8](=[O:19])[CH:9]=2)[CH2:13]1

Participants

3

Reactant 1

HCID 136238744HCID 136238744, compound

Product 1

HCID 136378672HCID 136378672, compound

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Procedure

A first enantiomer (1.1 g), [4-(2-methylmorpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetic acid ethyl ester −12°, c=2.047 mg/0.5 ml DMSO, 589 nm, the characteristics of which are:

Sources & evidence

ORD record
ord-c9ab927f86aa484da70ad70f2891e470
Source dataset
uspto-grants-2015_09
Patent number
US09133168B2

Reaction notes

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