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Ammonium Hydroxide → Chloromethyl tetrahydro-beta-carboline

HRID 2296241
Notes
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Reaction equation

HRID 2296241 reaction equation
Cl.[NH2:2][CH2:3][CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.COC(=O)[C:17]([CH2:19][Cl:20])=O.[OH-].[NH4+]>CO.[Cl-].[Na+].O>[Cl:20][CH2:19][CH:17]1[C:6]2[NH:7][C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:5]=2[CH2:4][CH2:3][NH:2]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 14923Ammonium HydroxideHCID 67652Tryptamine hydrochlorideHCID 12530121Methyl 3-chloro-2-oxopropanoate

Product 1

HCID 20472064Chloromethyl tetrahydro-beta-carbolineYield 77.4%

Reagents, catalysts & solvents 2

HCID 887MethanolSolvent
HCID 57417360
Sodium chloride; water
Solvent

Procedure

A susension of 108.4 g (0.55 mol) of tryptaminehydrochloride in 1 liter of dry methanol and 93.2 g (0.68 mol) of methyl-3-chloropyruvate* was refluxed under N2 for 24 h. The cooled mixture was poured into brine, made basic with ammonium hydroxide and extracted with dichloromethane. Concentration and trituration with ethyl acetate gave 94.0 g (61.3%) of the chloromethyl tetrahydro-β-carboline, melting point ("mp") 123°-125° C. The product was recrystallized from dichloromethane/pentane.

Workup

  1. extractionextracted with dichloromethane
  2. concentrationConcentration and trituration with ethyl acetate

Sources & evidence

ORD record
ord-e7764dee7b85473b9bb327f0cd07c941
Source dataset
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04428880

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes