HCID 14875694, compound → HCID 10878284, compound

HRID 1588332Notes

Reaction equation

HRID 1588332 reaction equation
C[CH:2]1[C:7](=[O:8])[NH:6][C:5]2[CH:9]=[CH:10][C:11]([C:13](=[O:16])[CH2:14][CH3:15])=[CH:12][C:4]=2[O:3]1.CC1(C)C(=O)NC2C=CC(C(=O)CC)=CC=2O1>>[O:16]=[C:13]([C:11]1[CH:10]=[CH:9][C:5]2[NH:6][C:7](=[O:8])[CH2:2][O:3][C:4]=2[CH:12]=1)[CH2:14][CH3:15]

Participants

3

Reactant 2

HCID 14875694HCID 14875694, compoundHCID 67884447HCID 67884447, compound

Product 1

HCID 10878284HCID 10878284, compound

Procedure

The following compounds were made by the above procedure, using the appropriate starting materials: 3,4-dihydro-2-methyl-7-(1-oxopropyl)-3-oxo-1,4(2H)-benzoxazine, mp 179°-179.5° C.; and 3,4-dihydro-2,2-dimethyl-7-(1-oxopropyl)-3-oxo-1,4(2H)-benzoxazine, mp 153°-155° C.

Sources & evidence

ORD record
ord-671c675767d042cfa90df22977468d58
Source dataset
uspto-grants-1993_06
Patent number
US05221742

Reaction notes

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