Benzyl Alcohol → HCID 15888183, compound

HRID 1107747Notes

Reaction equation

HRID 1107747 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[CH2:15][CH2:14]3)[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]([CH:13]3[CH2:15][CH2:14]3)[C:7]=12)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 18785707HCID 18785707, compound

Product 1

HCID 15888183HCID 15888183, compoundYield 78.6%

Procedure

The title compound was prepared as a white powder in 78.6% yield in a similar procedure to that described in Example 1 by using 7-chloro-1-cyclopropyl-2,3-dimethylpyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-62540bf93d234f12be7cad0d804e39c8
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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