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111661-47-3

111661-47-3 Structure

111661-47-3 Structure
IdentificationBack Directory
[Name]

4-METHYL-1,2,3,4-TETRAHYDRO-ISOQUINOLINE HYDROCHLORIDE
[CAS]

111661-47-3
[Synonyms]

4-Methyl-1,2,3,4-tetrahydroisoquinoline HCl
4-Methyl-1,2,3,4-tetrahydroisoquinoline HCl salt
1,2,3,4-tetrahydro-4-methylisoquinoline hydrochloride
4-METHYL-1,2,3,4-TETRAHYDRO-ISOQUINOLINE HYDROCHLORIDE
[Molecular Formula]

C10H14ClN
[MDL Number]

MFCD11501478
[MOL File]

111661-47-3.mol
[Molecular Weight]

183.68
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Safety DataBack Directory
[HS Code ]

2933499090
Hazard InformationBack Directory
[Uses]

1,2,3,4-Tetrahydro-4-methylisoquinoline Hydrochloride is a potent inhibitor of phenylethanolamine N-methyltransferase, an enzyme that catalyzes the formation of epinephrine.
[Synthesis]

4-Methylisoquinoline

1196-39-0

4-METHYL-1,2,3,4-TETRAHYDRO-ISOQUINOLINE HYDROCHLORIDE

111661-47-3

General procedure for the synthesis of 4-methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride from 4-methylisoquinoline: 0.50 g (3.5 mmol) of 4-methylisoquinoline was dissolved in 50 mL of methanol under a hydrogen atmosphere, and the hydrogenation reaction was carried out with the addition of 50 mg of dichloromethane and 3.5 mL of aqueous 1 M hydrochloric acid. Upon completion of the reaction, the catalyst was removed by diafiltration followed by evaporation of the reaction mixture. A mixture containing the starting material and the product was obtained, which could be used directly in the next step of the reaction without further purification. The yield was 0.60 g, which represents 94% of the theoretical yield.ESI-MS detection showed: m/z = 148 ([M + H]+).

[References]

[1] Patent: US2011/195954, 2011, A1. Location in patent: Page/Page column 104-105
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