3-tert-Butylbenzoyl chloride → HCID 44133905, compound

HRID 217866Notes

Reaction equation

HRID 217866 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][CH:20]=1)[O:5][C:6]1[C:15]2[N:14]=[C:13]([CH3:16])[C:12](=[O:17])[NH:11][C:10]=2[N:9]=[CH:8][CH:7]=1.[C:21]([C:25]1[CH:26]=[C:27]([CH:31]=[CH:32][CH:33]=1)[C:28](Cl)=[O:29])([CH3:24])([CH3:23])[CH3:22]>>[C:21]([C:25]1[CH:26]=[C:27]([CH:31]=[CH:32][CH:33]=1)[C:28]([NH:1][C:2]1[CH:20]=[CH:19][CH:18]=[C:4]([O:5][C:6]2[C:15]3[N:14]=[C:13]([CH3:16])[C:12](=[O:17])[NH:11][C:10]=3[N:9]=[CH:8][CH:7]=2)[CH:3]=1)=[O:29])([CH3:24])([CH3:22])[CH3:23]

Participants

3

Reactant 2

HCID 221431023-tert-Butylbenzoyl chlorideHCID 469015948-(3-aminophenoxy)-2-methylpyrido[2,3-b]pyrazin-3(4H)-one

Product 1

HCID 44133905HCID 44133905, compound

Procedure

Method G1 was used with 8-(3-aminophenoxy)-2-methylpyrido[2,3-b]pyrazin-3(4H)-one and 3-tertbutylbenzoyl chloride to afford the title compound as a slightly yellow solid (77 mg, 97%).

Sources & evidence

ORD record
ord-f623b0c458ed43a6ba38e1d9331e0404
Source dataset
uspto-grants-2012_06
Patent number
US08198279B2

Reaction notes

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