HCID 10947253, compound → HCID 21310720, compound

HRID 583186Notes

Reaction equation

HRID 583186 reaction equation
[Br:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[CH:5]=[C:4]([NH2:12])[CH:3]=1.BrC1C=C(N2[C:24]([C:25]([F:28])([F:27])[F:26])=[N:23][N:22]=[N:21]2)C=CC=1OC>>[Br:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[CH:5]=[C:4]([N:12]2[C:24]([C:25]([F:28])([F:27])[F:26])=[N:23][N:22]=[N:21]2)[CH:3]=1

Participants

3

Reactant 2

HCID 10947253HCID 10947253, compoundHCID 21310721HCID 21310721, compound

Product 1

HCID 21310720HCID 21310720, compound

Procedure

Compound was prepared according to the procedure given in Example 6, Step F (b & c) using 4-bromo-2-methyl-6-amino-benzooxazole in place of 2-Bromo-4-(trifluoroacetamido)anisole and 2-Bromo-4-(5-(trifluoromethyl)tetrazol-1-yl)anisole.

Workup

  1. customCompound was prepared

Sources & evidence

ORD record
ord-d6d63324b5cf439d82a9f695aefa0952
Source dataset
uspto-grants-1999_07
Patent number
US05929094

Reaction notes

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