HCID 12216921, compound → HCID 19082331, compound

HRID 1741656Notes

Reaction equation

HRID 1741656 reaction equation
[CH3:1][O:2][C:3]([O:5][N:6]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][C:26]2[N:27]=[C:28]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[O:29][C:30]=2[CH3:31])=[CH:19][CH:18]=1)[C:7]([NH:9][C:10]1[CH:15]=CC=C[CH:11]=1)=[O:8])=[O:4].C1(N(O)C(N)=O)C=CC=CC=1>>[CH3:15][CH:10]([NH:9][C:7]([N:6]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][C:26]2[N:27]=[C:28]([C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)[O:29][C:30]=2[CH3:31])=[CH:19][CH:18]=1)[O:5][C:3]([O:2][CH3:1])=[O:4])=[O:8])[CH3:11]

Participants

3

Reactant 2

HCID 12216921HCID 12216921, compoundHCID 19082322HCID 19082322, compound

Product 1

HCID 19082331HCID 19082331, compound

Procedure

By the same method, N-(methoxycarbonyloxy)-N-(phenylaminocarbonyl)-4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylamine is prepared from the corresponding phenyl-hydroxyurea of Preparation J.

Sources & evidence

ORD record
ord-d33a9d6954b6493db9e20455e3e4084d
Source dataset
uspto-grants-1994_08
Patent number
US05334604

Reaction notes

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