Benzyl Alcohol → HCID 15888180, compound

HRID 1107745Notes

Reaction equation

HRID 1107745 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]=[CH2:14])[C:7]=12.[CH2:15]([OH:22])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH2:15]([O:22][C:2]1[N:3]=[N:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[N:8]([CH:13]=[CH2:14])[C:7]=12)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 18785682HCID 18785682, compound

Product 1

HCID 15888180HCID 15888180, compoundYield 59.7%

Procedure

The title compound was prepared as a white powder in 59.7% yield in a similar procedure to that described in Example 1 by using 7-chloro-2,3-dimethyl-1-vinylpyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-dced6a60c50c465d87e8043bc2fabf8c
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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