4-(Chloromethyl)pyridinium chloride → HCID 19040653, compound

HRID 1683762Notes

Reaction equation

HRID 1683762 reaction equation
Cl[CH2:2][C:3]1[O:4][CH:5]=[CH:6][CH:7]=1.BrCC1C=COC=1.ClC[CH:17]=[CH:18][C:19]1O[CH:21]=[CH:22][CH:23]=1.BrCC1SC=CC=1.BrCC1C=CSC=1.CC1C=CC(S(O[CH2:49][CH2:50][N:51]2[CH:55]=[CH:54]C=N2)(=O)=O)=CC=1.Cl[CH2:57][N:58]1[CH:62]=NC=N1.Cl.[Cl:64]CC1C=CN=CC=1>>[Cl:64][C:23]1[C:19]2[CH2:18][CH2:17][N:58]([CH3:62])[CH2:57][CH2:7][C:6]=2[C:5]([O:4][CH2:3][C:2]2[CH:49]=[CH:50][N:51]=[CH:55][CH:54]=2)=[CH:21][CH:22]=1

Participants

9

Reactant 8

HCID 745704-(Chloromethyl)pyridinium chlorideHCID 2195202-(Chloromethyl)furanHCID 5207033-(Bromomethyl)thiopheneHCID 37438821-Chloromethyl-1H-1,2,4-triazoleHCID 110949343-(Bromomethyl)furanHCID 118299782-(Bromomethyl)thiopheneHCID 19040641HCID 19040641, compoundHCID 54215427HCID 54215427, compound

Product 1

HCID 19040653HCID 19040653, compound

Procedure

Using the general procedure of Example 2, replacing 1-(chloromethyl)-1H-pyrazole with 2-(chloromethyl)furan, 3-(bromomethyl) furan, 2-(3-chloro-1-propenyl)furan, 2-(bromomethyl)thiophene, 3-(bromomethyl)thiophene, 2-(1H-pyrazol-1-yl)ethyl 4-methylbenzenesulfonate, 1-(chloro-methyl)-1H-1,2,4-triazole, and 4-(chloromethyl)pyridine hydrochloride gave:

Workup

  1. customgave

Sources & evidence

ORD record
ord-211bd68e84fb450ea248c50fdad8ef86
Source dataset
uspto-grants-1997_06
Patent number
US05639748

Reaction notes

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