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Sodium → HCID 20155386, 화합물

HRID 2413719
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HRID 2413719 반응식
[Na].[CH2:2]([O:9][C:10]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:11]=1[C:12]1[C:13]([CH2:35][O:36][CH3:37])=[C:14]([CH:33]=[CH2:34])[N:15]=[CH:16][C:17]=1[N:18]2S(C1C=CC(C)=CC=1)(=O)=O)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>CO>[CH2:2]([O:9][C:10]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:11]=1[C:12]1[C:13]([CH2:35][O:36][CH3:37])=[C:14]([CH:33]=[CH2:34])[N:15]=[CH:16][C:17]=1[NH:18]2)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5360545SodiumHCID 20155385HCID 20155385, 화합물

생성물 1

HCID 20155386HCID 20155386, 화합물수율 39.1%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of 0.23 g of sodium in 10 ml of methanol is added drop by drop with stirring to a suspension of 0.5 g of 5-benzyloxy-4-methoxymethyl-9-tosyl-3-vinyl-beta-carboline in 20 ml of methanol. After 72 hours of stirring at room temperature, it is evaporated to dryness and the residue is chromatographed over silica gel with dichloromethane/ethanol=10/1 as eluant. 0.135 g of 5-benzyloxy-4-methoxymethyl-3-vinyl-beta-carboline with a melting point of 183°-185° C. is obtained.

후처리

  1. customit is evaporated to dryness
  2. customthe residue is chromatographed over silica gel with dichloromethane/ethanol=10/1 as eluant

출처 및 근거

ORD 기록
ord-1cca7dd45f3649318356876b1c93e809
출처 데이터셋
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04719210

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