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

HRID 108359Notes

Reaction equation

HRID 108359 reaction equation
[CH2:1]([CH3:2])[O:3][c:4]1[cH:5][cH:6][c:7]2[cH:8][cH:9][c:10]([B:14]3[O:15][C:16]([CH3:17])([CH3:18])[C:19]([CH3:20])([CH3:21])[O:22]3)[cH:11][c:12]2[cH:13]1.[Cl:23][c:24]1[cH:25][c:26]([CH2:30][n:31]2[c:32]([CH3:36])[n:33][cH:34][cH:35]2)[n:27][n:28][cH:29]1>>[CH2:1]([CH3:2])[O:3][c:4]1[cH:5][cH:6][c:7]2[cH:8][cH:9][c:10](-[c:24]3[cH:25][c:26]([CH2:30][n:31]4[c:32]([CH3:36])[n:33][cH:34][cH:35]4)[n:27][n:28][cH:29]3)[cH:11][c:12]2[cH:13]1.[ClH:23]

Participants

4

Reactant 2

HCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazineHCID 222402002-(7-Ethoxynaphthalen-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

Product 2

HCID 313Hydrochloric AcidHCID 222402345-(7-Ethoxynaphthalen-2-yl)-3-[(2-methylimidazol-1-yl)methyl]pyridazine

Sources & evidence

ORD record
ord-cdd52aba8a0b49329d0f5f51fca55c75
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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