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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 350083, 화합물 → HCID 13209120, 화합물

HRID 615522
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HRID 615522 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][CH:13]=1>O1CCCC1.[Pd]>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH2:10][CH2:11][C:12]1[CH:13]=[CH:14][C:15]([NH2:18])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 350083HCID 350083, 화합물

생성물 1

HCID 13209120HCID 13209120, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 23938Palladium용매

실험 절차

150 parts by weight of β-(benzothiazol-2-yl)-4-nitrostyrene were dissolved in 1,500 parts by volume of tetrahydrofuran, and 15 parts by weight of Pd/C (10%) were added. After the mixture had been flushed with nitrogen, hydrogen was passed in. After some hours, the uptake of hydrogen (44 1) had ended, and the mixture was flushed with nitrogen again, the catalyst was filtered off and the filtrate was concentrated. 135.6 g of 4-(β-benzothiazol-2-yl-ethyl)-aniline of melting point 79°-81° C. were obtained.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
addition
were added
  • customAfter the mixture had been flushed with nitrogen, hydrogen
  • waitAfter some hours
  • customthe mixture was flushed with nitrogen again
  • filtrationthe catalyst was filtered off
  • concentrationthe filtrate was concentrated
  • 출처 및 근거

    ORD 기록
    ord-0a06d3a484b54c3eb1e142a6f0ed42be
    출처 데이터셋
    uspto-grants-1985_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04500340

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