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Indole-3-pyruvic acid → HCID 12457675, 화합물

HRID 359725
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인쇄 미리보기

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HRID 359725 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11](=[O:15])[C:12]([OH:14])=[O:13])=[CH:2]1.[CH2:16]1CCN2C(=NCCC2)C[CH2:17]1.C(Br)C>C1C=CC=CC=1>[CH2:16]([O:13][C:12](=[O:14])[C:11]([CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1)=[O:15])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 803Indole-3-pyruvic acidHCID 6332Ethyl BromideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

생성물 1

HCID 12457675HCID 12457675, 화합물수율 70%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

Following the same method as previously described, 1,0 g 3-indole-pyruvic acid were reacted with 1,5 ml DBU and 790 microliters ethylbromide. In this case the benzene solution appeared red orange. After flash chromatography purification the ethyl ester was obtained with a yield of about 70%.

후처리

  1. customAfter flash chromatography purification the ethyl ester
  2. customwas obtained with a yield of about 70%

출처 및 근거

ORD 기록
ord-b950a389228e4d7da502945220a05509
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05002963

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