5-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine → Hydrochloric Acid

Reaction equation

[CH3:1][O:2][c:3]1[c:4]([B:13]2[O:14][C:15]([CH3:16])([CH3:17])[C:18]([CH3:19])([CH3:20])[O:21]2)[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1.[Cl:22][c:23]1[cH:24][c:25]([CH2:29][n:30]2[c:31]([CH3:35])[n:32][cH:33][cH:34]2)[n:26][n:27][cH:28]1>>[CH3:1][O:2][c:3]1[c:4](-[c:23]2[cH:24][c:25]([CH2:29][n:30]3[c:31]([CH3:35])[n:32][cH:33][cH:34]3)[n:26][n:27][cH:28]2)[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1.[ClH:22]

Participants

Reactant 2

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

HCID 219239592-(2-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Product 2

HCID 313Hydrochloric Acid

HCID 22240277HCID 22240277, compound

Sources & evidence

ORD record: ord-914f47ae4514469f84946de5e1cf899d
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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