3-Bromoaniline → HCID 60113814, compound

HRID 852325Notes

Reaction equation

HRID 852325 reaction equation
Cl[C:2]1[CH:3]=[C:4]([N:8]2[N:12]=[N:11][C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)=[N:9]2)[CH:5]=[CH:6][CH:7]=1.[Br:19]C1C=C(C=CC=1)N.N1C=CC=CC=1C=O>>[Br:19][C:2]1[CH:3]=[C:4]([N:8]2[N:12]=[N:11][C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)=[N:9]2)[CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 115623-BromoanilineHCID 142732-PyridinecarboxaldehydeHCID 99213692-[2-(3-chlorophenyl)-2H-tetrazol-5-yl]pyridine

Product 1

HCID 60113814HCID 60113814, compound

Procedure

Following the procedure described in EXAMPLE 1 for the synthesis of 2-[2-(3-chlorophenyl)-2H-tetrazol-5-yl]pyridine, 3-bromoaniline (223 mg, 1.3 mmol) and pyridine-2-carboxaldehyde (135 mg, 1.3 mmol) were employed to obtain 2-[2-(3-bromophenyl)-2H-tetrazol-5-yl]pyridine as an orange solid.

Sources & evidence

ORD record
ord-91227a3cca1e4d1a97e9cec9a7a0cf89
Source dataset
uspto-grants-2007_08
Patent number
US07253190B2

Reaction notes

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