3,5-Dimethyl-4-hydroxybenzaldehyde → HCID 15516464, compound

HRID 1976196Notes

Reaction equation

HRID 1976196 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([CH3:11])[C:9]=1[OH:10])[CH:5]=O.[CH2:12]([NH:19][S:20]([CH2:23][C:24]#[N:25])(=[O:22])=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[CH2:12]([NH:19][S:20](/[C:23](=[CH:5]/[C:4]1[CH:3]=[C:2]([CH3:1])[C:9]([OH:10])=[C:8]([CH3:11])[CH:7]=1)/[C:24]#[N:25])(=[O:22])=[O:21])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Participants

3

Reactant 2

HCID 752223,5-Dimethyl-4-hydroxybenzaldehydeHCID 15410493HCID 15410493, compound

Product 1

HCID 15516464HCID 15516464, compound

Procedure

The titled compound was prepared with 3,5-dimethyl-4-hydroxybenzaldehyde and N-benzyl cyanomethylsulfonamide under the similar conditions as described for EXAMPLE 12 (part B).

Sources & evidence

ORD record
ord-8058270f5b0a424681268705d5eea892
Source dataset
uspto-grants-2001_05
Patent number
US06225346B1

Reaction notes

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