Pyridine → HCID 67427596, compound

HRID 154739Notes

Reaction equation

HRID 154739 reaction equation
[CH2:38]([Cl:39])[Cl:40].[CH3:1][C:2]1([CH3:14])[C:3](=[O:13])[c:4]2[c:5]([s:6][c:7]([C:9](=[O:10])[OH:11])[cH:8]2)[CH2:12]1.[F:15][c:16]1[c:17]([NH2:18])[cH:19][c:20]([B:23]2[O:24][C:25]([CH3:30])([CH3:31])[C:26]([CH3:28])([CH3:29])[O:27]2)[cH:21][cH:22]1.[cH:32]1[cH:33][cH:34][n:35][cH:36][cH:37]1>>[CH3:1][C:2]1([CH3:14])[C:3](=[O:13])[c:4]2[c:5]([s:6][c:7]([C:9](=[O:11])[NH:18][c:17]3[c:16]([F:15])[cH:22][cH:21][c:20]([B:23]4[O:24][C:25]([CH3:30])([CH3:31])[C:26]([CH3:28])([CH3:29])[O:27]4)[cH:19]3)[cH:8]2)[CH2:12]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 467379902-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 58540128HCID 58540128, compound

Product 1

HCID 67427596HCID 67427596, compound

Sources & evidence

ORD record
ord-341df5b299264022864fadf36e60ab76
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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