2,3-Dichloropyridine → HCID 178496128, compound

HRID 2018885Notes

Reaction equation

HRID 2018885 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][O:5][c:6]1[cH:11][cH:10][c:9]([C:12]([NH:14][C@H:15]2[CH2:20][N:19]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:18][CH2:17][CH2:16]2)=[O:13])[cH:8][cH:7]1.[Cl:28][c:29]1[c:34](Br)[n:33][cH:32][cH:31][cH:30]1.Clc1c(Cl)nccc1>>[CH3:1][O:2][CH2:3][CH2:4][O:5][c:6]1[cH:11][cH:10][c:9]([C:12]([N:14]([c:34]2[c:29]([Cl:28])[cH:30][cH:31][cH:32][n:33]2)[C@H:15]3[CH2:20][N:19]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:18][CH2:17][CH2:16]3)=[O:13])[cH:8][cH:7]1

Participants

7

Reactant 3

HCID 169882,3-DichloropyridineHCID 70163262-Bromo-3-chloropyridineHCID 178496130HCID 178496130, compound

Product 1

HCID 178496128HCID 178496128, compound

Reagents, catalysts & solvents 3

HCID 3251421Potassium bis(trimethylsilyl)amideReagentHCID 1140TolueneSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
130 °C

Sources & evidence

ORD record
ord-f30cdd908bf7447b8dd9c38be013717d
Source dataset
39k HTE dataset from Pfizer
Original link
View source

Reaction notes

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