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Ammonium Hydroxide → Chloromethyl tetrahydro-beta-carboline

HRID 2296241
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인쇄 미리보기

반응식

HRID 2296241 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

HCID 20472064Chloromethyl tetrahydro-beta-carboline수율 77.4%

시약·촉매·용매 2

HCID 887Methanol용매HCID 57417360Sodium chloride; water용매
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실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-e7764dee7b85473b9bb327f0cd07c941
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04428880

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