2-Fluoro-4,5-dimethoxybenzaldehyde → HCID 86617923, compound

HRID 1161551Notes

Reaction equation

HRID 1161551 reaction equation
[CH3:1][O:2][C:3](=[O:29])[N:4]=[C:5]([S:27][CH3:28])[C:6](=[N:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]#[N:26])=[CH:21][CH:20]=1)[C:7]1[CH:12]=[C:11]([O:13][CH3:14])[CH:10]=[C:9](OC)[C:8]=1[F:17].FC1C=C(OC)C(OC)=CC=1[CH:33]=[O:34]>>[CH3:1][O:2][C:3](=[O:29])[N:4]=[C:5]([S:27][CH3:28])[C:6](=[N:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]#[N:26])=[CH:21][CH:20]=1)[C:7]1[CH:12]=[C:11]([O:13][CH3:14])[C:10]([O:34][CH3:33])=[CH:9][C:8]=1[F:17]

Participants

3

Reactant 2

HCID 6035952-Fluoro-4,5-dimethoxybenzaldehydeHCID 72312730HCID 72312730, compound

Product 1

HCID 86617923HCID 86617923, compound

Procedure

The same procedure was carried out as in Example (2a) to (2e), except that 2-fluoro-4,5-dimethoxybenzaldehyde was used instead of the 2-fluoro-3,5-dimethoxybenzaldehyde in Example (2a), to give [2-(4-Cyanophenylimino)-2-(2-fluoro-4,5-dimethoxyphenyl)-1-methylsulfanylethylidene]carbamic acid methyl ester.

Sources & evidence

ORD record
ord-db0ef226f18b4a1ca61ba35c10614ddd
Source dataset
uspto-grants-2010_10
Patent number
US07816522B2

Reaction notes

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