p-Anisoyl chloride → HCID 69070047, compound

HRID 229396Notes

Reaction equation

HRID 229396 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][C:20]([O:23][CH3:24])=[CH:19][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][C:20]([O:23][CH3:24])=[CH:19][CH:18]=1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 69071092HCID 69071092, compound

Product 1

HCID 69070047HCID 69070047, compound

Procedure

7-Fluoro-5-(4-methoxybenzoyl)-4-methyl-4,5-dihydropyrrolo[1,2-a]quinoxaline was prepared from the product of Example 47 and p-anisoyl chloride according to the procedure of Example 106, Step 2. MS (ESI) m/z 337; Anal. Calcd for C20H17FN2O2: C, 71.42; H, 5.09; N, 8.33. Found: C, 70.89; H, 4.96; N, 8.01.

Sources & evidence

ORD record
ord-81d1117e231543f98553c6868047f64c
Source dataset
uspto-grants-2009_07
Patent number
US07563793B2

Reaction notes

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