Furan-2-boronic acid → HCID 54198063, compound

HRID 581938Notes

Reaction equation

HRID 581938 reaction equation
C([N:4]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N:21]2[CH:25]=[CH:24][N:23]=[CH:22]2)[CH:16]=1)[C:5]1[CH:10]=[CH:9][C:8](I)=[CH:7][C:6]=1[N+:12]([O-:14])=[O:13])(=O)C.[O:26]1[CH:30]=[CH:29][CH:28]=[C:27]1B(O)O>>[N:21]1([C:17]2[CH:16]=[C:15]([NH:4][C:5]3[CH:10]=[CH:9][C:8]([C:27]4[O:26][CH:30]=[CH:29][CH:28]=4)=[CH:7][C:6]=3[N+:12]([O-:14])=[O:13])[CH:20]=[CH:19][CH:18]=2)[CH:25]=[CH:24][N:23]=[CH:22]1

Participants

3

Reactant 2

HCID 2734357Furan-2-boronic acidHCID 53867634HCID 53867634, compound

Product 1

HCID 54198063HCID 54198063, compoundYield 77%

Procedure

N-(3-(1-Imidazolyl)phenyl)-4-(2-furanyl)-2-nitroaniline (7o) was prepared analogously from 6c (Example 8) and 2-furanylboronic acid. Yield: 77%. Mp 147-149° C.

Sources & evidence

ORD record
ord-57d16360539b470abe948d1c92121693
Source dataset
uspto-grants-1999_07
Patent number
US05922724

Reaction notes

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