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1-Azido-4-nitrobenzene → HCID 68852179, 화합물

HRID 1473846
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인쇄 미리보기

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HRID 1473846 반응식
[N:1]([C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][CH:5]=1)=[N+:2]=[N-:3].[CH3:13][Si:14]([C:17]#[C:18][N:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1)([CH3:16])[CH3:15]>C1(C)C=CC=CC=1>[N+:10]([C:7]1[CH:8]=[CH:9][C:4]([N:1]2[C:18]([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)=[C:17]([Si:14]([CH3:16])([CH3:15])[CH3:13])[N:3]=[N:2]2)=[CH:5][CH:6]=1)([O-:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1370491-Azido-4-nitrobenzeneHCID 114694704-[(Trimethylsilyl)ethynyl]morpholine

생성물 1

HCID 68852179HCID 68852179, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
60 °C

실험 절차

A mixture of 1-azido-4-nitrobenzene (0.5 g, 3.0 mmol), 4-((trimethylsilyl)ethynyl)morpholine (1.0 g, 9.0 mmol) and toluene (10 mL) was heated in a sealed tube to 60° C. for 24 h. The reaction mixture was concentrated in vacuo to give 4-(1-(4-nitrophenyl)-4-(trimethylsilyl)-1H-1,2,3-triazol-5-yl)morpholine which was further reduced following procedure D to afford 4-(5-morpholino-4-(trimethylsilyl)-1H-1,2,3-triazol-1-yl)aniline.

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-d697923a3ed74c449917bd606416fb1b
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018205B2

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