Benzyl Alcohol → HCID 18785697, compound

HRID 1107737Notes

Reaction equation

HRID 1107737 reaction equation
Cl[C:2]1[N:3]=[N:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[N:8]([CH2:13][CH:14]=[CH2:15])[C:7]=12.[CH2:16]([OH:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:16]([O:23][C:2]1[N:3]=[N:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[N:8]([CH2:13][CH:14]=[CH2:15])[C:7]=12)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 18785586HCID 18785586, compound

Product 1

HCID 18785697HCID 18785697, compoundYield 63.2%

Procedure

The title compound was prepared as a white powder in 63.2% yield in a similar procedure to that described in Example 1 by using 7-chloro-2,3-dimethyl-1-(2-propenyl)pyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-89cf84d222eb4f72aca1656da6b904ef
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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