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Ammonium Hydroxide → Chloromethyl tetrahydro-beta-carboline

HRID 1902254
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반응식

HRID 1902254 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 suspension 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. temperaturewas refluxed under N2 for 24 h
  2. extractionextracted with dichloromethane
  3. concentrationConcentration and trituration with ethyl acetate

출처 및 근거

ORD 기록
ord-aca795ff1c6743918c9c5449702998c6
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04362739

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