Benzyl Alcohol → HCID 15888189, compound

HRID 1107754Notes

Reaction equation

HRID 1107754 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]([CH:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[C:7]=12.[CH2:19]([OH:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:19]([O:26][C:2]1[N:3]=[N:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[N:8]([CH:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[C:7]=12)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 18785704HCID 18785704, compound

Product 1

HCID 15888189HCID 15888189, compoundYield 92.8%

Procedure

The title compound was prepared as a white powder in 92.8% yield in a similar procedure to that described in Example 1 by using 7-chloro-1-cyclohexyl-2,3-dimethylpyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-ee53b30e4a6e464b9ae5f9df479a546b
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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