Allyl Alcohol → HCID 23020476, compound

HRID 747157Notes

Reaction equation

HRID 747157 reaction equation
Cl[C:2]1[C:7]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=2)=[C:6]([C:14]2[O:15][CH:16]=[CH:17][CH:18]=2)[N:5]=[C:4]([NH2:19])[N:3]=1.[CH2:20]([OH:23])[CH:21]=[CH2:22]>>[CH2:20]([O:23][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=2)=[C:6]([C:14]2[O:15][CH:16]=[CH:17][CH:18]=2)[N:5]=[C:4]([NH2:19])[N:3]=1)[CH:21]=[CH2:22]

Participants

3

Reactant 2

HCID 7858Allyl AlcoholHCID 23020421HCID 23020421, compound

Product 1

HCID 23020476HCID 23020476, compound

Procedure

The title compound was synthesized in a similar manner to Example 3 using 4-chloro-6-(2-furyl)-5-(4-pyridyl)-2-pyrimidinylamine and allyl alcohol.

Sources & evidence

ORD record
ord-d751e7a138cd4ca0a16fe4d7066d12e2
Source dataset
uspto-grants-2008_07
Patent number
US07396836B2

Reaction notes

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