Phenylboronic Acid → HCID 22240249, compound

HRID 891880Notes

Reaction equation

HRID 891880 reaction equation
[C:1]1(B(O)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:10][C:11]1[CH:12]=[C:13]([CH2:17][N:18]2[CH:22]=[CH:21][N:20]=[C:19]2[CH3:23])[N:14]=[N:15][CH:16]=1>>[ClH:10].[CH3:23][C:19]1[N:18]([CH2:17][C:13]2[N:14]=[N:15][CH:16]=[C:11]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[CH:12]=2)[CH:22]=[CH:21][N:20]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine

Product 1

HCID 22240249HCID 22240249, compound

Procedure

The title compound, MS: m/e=251.2 (M+H+), was prepared from phenylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-ylmethyl)-pyridazine.

Sources & evidence

ORD record
ord-fe11a054fd324ace9716dfdd52a8a4da
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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