Benzyl Alcohol → HCID 15888185, compound

HRID 1107749Notes

Reaction equation

HRID 1107749 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][CH2:14][F: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][CH2:14][F: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 18785600HCID 18785600, compound

Product 1

HCID 15888185HCID 15888185, compoundYield 76.2%

Procedure

The title compound was prepared as white crystals in 76.2% yield in a similar procedure to that described in Example 1 by using 7-chloro-1-(2-fluoroethyl)-2,3-dimethylpyrrolo[2,3-d]pyridazine and benzyl alcohol.

Sources & evidence

ORD record
ord-1fd2427b5c594f76a94bee1f8f48b428
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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