2-Pyridinecarboxaldehyde → HCID 9834844, compound

HRID 852329Notes

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.[CH3:19][O:20]C1C=CC=CC=1NC1C=CC=CC=1.N1C=CC=CC=1C=O>>[CH3:19][O:20][C:5]1[CH:6]=[CH:7][CH:2]=[CH:3][C:4]=1[N:8]1[N:12]=[N:11][C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)=[N:9]1

Participants

Reactant 3

HCID 142732-Pyridinecarboxaldehyde

HCID 99213692-[2-(3-chlorophenyl)-2H-tetrazol-5-yl]pyridine

HCID 109105142-methoxyphenylaniline

Product 1

HCID 9834844HCID 9834844, compound

Procedure

Following the procedure described in EXAMPLE 1 for the synthesis of 2-[2-(3-chlorophenyl)-2H-tetrazol-5-yl]pyridine, 2-methoxyphenylaniline (36.9 mg, 0.3 mmol) and 2-pyridinecarboxaldehyde (32.1 mg, 0.3 mmol) were employed to obtain 2-[2-(2-methoxyphenyl)-2H-tetrazol-5-yl]pyridine as an orange solid.

Sources & evidence

ORD record: ord-7077592231714ff790072df13bb53d12
Source dataset: uspto-grants-2007_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07253190B2

Reaction notes

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