1-Naphthaleneboronic acid → HCID 22240197, compound

HRID 891883Notes

Reaction equation

HRID 891883 reaction equation
[C:1]1(B(O)O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[Cl:14][C:15]1[CH:16]=[C:17]([CH2:21][N:22]2[CH:26]=[CH:25][N:24]=[C:23]2[CH3:27])[N:18]=[N:19][CH:20]=1>>[ClH:14].[CH3:27][C:23]1[N:22]([CH2:21][C:17]2[N:18]=[N:19][CH:20]=[C:15]([C:2]3[CH:3]=[CH:4][C:5]4[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=4)[CH:1]=3)[CH:16]=2)[CH:26]=[CH:25][N:24]=1

Participants

3

Reactant 2

HCID 2545321-Naphthaleneboronic acidHCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine

Product 1

HCID 22240197HCID 22240197, compound

Procedure

The title compound, MS: m/e=301.3 (M+H+), was prepared from naphtylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Sources & evidence

ORD record
ord-eb69b21477e9457f8042b9e642977be8
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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