N-Methoxy-N-methylbutyramide → HCID 67466928, compound

HRID 1619948Notes

Reaction equation

HRID 1619948 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[O:16][C:17]3[CH:23]=[C:22](Br)[CH:21]=[CH:20][C:18]=3[N:19]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CON(C)[C:28](=[O:32])[CH2:29][CH2:30][CH3:31]>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[O:16][C:17]3[CH:23]=[C:22]([C:28](=[O:32])[CH2:29][CH2:30][CH3:31])[CH:21]=[CH:20][C:18]=3[N:19]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 13704543N-Methoxy-N-methylbutyramideHCID 67465270HCID 67465270, compound

Product 1

HCID 67466928HCID 67466928, compound

Procedure

The preparation is carried out analogously to Example 29a from 2-(4-benzyloxy-phenyl)-6-bromo-benzoxazole and N-methoxy-N-methyl-butyramide.

Sources & evidence

ORD record
ord-246d5d64d4554576ab1af8294cac9ed1
Source dataset
uspto-grants-2014_07
Patent number
US08772323B2

Reaction notes

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