m-Anisoyl chloride → HCID 69067156, compound

HRID 229399Notes

Reaction equation

HRID 229399 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[CH:12]=[CH:13][CH:14]=[C:7]1[CH:6]([CH3:15])[NH:5]2.[C:16](Cl)(=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH3:24])[CH:18]=1>>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[CH:12]=[CH:13][CH:14]=[C:7]1[CH:6]([CH3:15])[N:5]2[C:16](=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH3:24])[CH:18]=1

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 69071092HCID 69071092, compound

Product 1

HCID 69067156HCID 69067156, compound

Procedure

7-Fluoro-5-(3-methoxybenzoyl)-4-methyl-4,5-dihydropyrrolo[1,2-a]quinoxaline was prepared from the product of Example 47 and m-anisoyl chloride according to the procedure of Example 106, Step 2. MS (ESI) m/z 337.

Sources & evidence

ORD record
ord-19d650d959d34830b5286dcfda6999de
Source dataset
uspto-grants-2009_07
Patent number
US07563793B2

Reaction notes

Loading…