Benzyl Alcohol → HCID 15888169, compound

HRID 1107736Notes

Reaction equation

HRID 1107736 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]=[C:15]([CH3:17])[CH3:16])[C:7]=12.[CH2:18]([OH:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH2:18]([O:25][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]=[C:15]([CH3:17])[CH3:16])[C:7]=12)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 18785585HCID 18785585, compound

Product 1

HCID 15888169HCID 15888169, compound

Procedure

The title compound was prepared as a white powder in -6.2% yeild in a similar procedure to that described in Example 1 by using 7-chloro-2,3-dimethyl-1-(3-methyl-2-butenyl)pyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-8d474c5ef9d24f14b4646eac99eae043
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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