Pyridine → HCID 53234455, compound

HRID 2146508Notes

Reaction equation

HRID 2146508 reaction equation
[Cl:18][S:19](=[O:20])(=[O:21])[c:22]1[c:23]([CH2:35][C:36](=[O:37])[O:38][CH2:39][CH3:40])[cH:24][c:25]([NH:28][C:29]([C:30]([F:31])([F:32])[F:33])=[O:34])[cH:26][cH:27]1.[Cl:41][CH2:42][Cl:43].[NH2:1][c:2]1[cH:3][cH:4][c:5]2[c:6]([cH:11]1)[B:7]([OH:10])[O:8][CH2:9]2.[cH:12]1[cH:13][cH:14][n:15][cH:16][cH:17]1>>[NH:1]([c:2]1[cH:3][cH:4][c:5]2[c:6]([cH:11]1)[B:7]([OH:10])[O:8][CH2:9]2)[S:19](=[O:20])(=[O:21])[c:22]1[c:23]([CH2:35][C:36](=[O:37])[O:38][CH2:39][CH3:40])[cH:24][c:25]([NH:28][C:29]([C:30]([F:31])([F:32])[F:33])=[O:34])[cH:26][cH:27]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 37701876-Aminobenzo(c)(1,2)oxaborol-1(3H)-olHCID 86655216HCID 86655216, compound

Product 1

HCID 53234455HCID 53234455, compound

Sources & evidence

ORD record
ord-cad38d5f3e794b58b331760171297b10
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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