2-Aminopyridine → HCID 21495122, compound

HRID 267968Notes

Reaction equation

HRID 267968 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:8][CH2:9][S:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[Br:17]>C1(C)C(C)=CC=CC=1>[Cl-:8].[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[CH2:9][S:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[Br:17]

Participants

4

Reactant 2

HCID 104392-AminopyridineHCID 218284941-Bromo-2-[(chloromethyl)sulfanyl]benzene

Product 1

HCID 21495122HCID 21495122, compoundYield 81.5%

Reagents, catalysts & solvents 1

HCID 7237O-XyleneSolvent2×

Procedure

To a solution of 14.1 g of 2-aminopyridine in 180 ml of xylene is added a solution of 24.0 g of o-bromophenyl chloromethyl sulfide in 40 ml of xylene. The mixture is heated at 90°-95° for about fifteen hours to give about 27.3 g of the named compound, mp about 199°-201°.

Workup

  1. temperatureThe mixture is heated at 90°-95° for about fifteen hours

Sources & evidence

ORD record
ord-eca9c38d06d543cf9dc72fa177bfb35b
Source dataset
uspto-grants-1976_03
Patent number
US03946025

Reaction notes

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