2,4-Dichloro-6-methoxy-3,5-triazine → HCID 86640786, compound

HRID 1942901Notes

Reaction equation

HRID 1942901 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[C:11]([CH2:13][OH:14])[N:10]=[CH:9]2)=[C:4]([O:15][CH3:16])[CH:3]=1.[Cl:17][C:18]1[N:23]=[C:22](Cl)[N:21]=[C:20]([O:25][CH3:26])[N:19]=1>C(N(CC)CC)C>[Cl:17][C:18]1[N:19]=[C:20]([O:25][CH3:26])[N:21]=[C:22]([NH:1][C:2]2[CH:7]=[CH:6][C:5]([N:8]3[CH:12]=[C:11]([CH2:13][OH:14])[N:10]=[CH:9]3)=[C:4]([O:15][CH3:16])[CH:3]=2)[N:23]=1

Participants

4

Reactant 2

HCID 192672,4-Dichloro-6-methoxy-3,5-triazineHCID 66886492HCID 66886492, compound

Product 1

HCID 86640786HCID 86640786, compoundYield 61%

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

This compound was prepared in analogy to example 8 from [1-(4-amino-2-methoxy-phenyl)-1H-imidazol-4-yl]-methanol, triethylamine and 2,4-dichloro-6-methoxy-1,3,5-triazine. The title compound was isolated as a brownish solid in 61% yield.

Sources & evidence

ORD record
ord-17a3775351bc43038a2f9be4f68fb04d
Source dataset
uspto-grants-2013_03
Patent number
US08389717B2

Reaction notes

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