홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Phenazine → 2,3-dimethylbenzo(B)phenazine

HRID 610778
노트
인쇄 미리보기

반응식

HRID 610778 반응식
[NH2:1][C:2]1[C:11]([NH2:12])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[CH3:13][C:14]1[C:19]([CH3:20])=[CH:18][C:17](=O)[C:16](=O)[CH:15]=1.C1C2C(=NC3C(N=2)=CC=CC=3)C=CC=1.IC>C(O)(=O)C.C(O)C>[CH3:13][C:14]1[C:19]([CH3:20])=[CH:18][C:17]2[N:1]=[C:2]3[C:11](=[N:12][C:16]=2[CH:15]=1)[CH:10]=[C:9]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]1=[CH:3]3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 4757PhenazineHCID 6328Methyl iodideHCID 698722,3-DiaminonaphthaleneHCID 122947044,5-Dimethyl-1,2-benzoquinone

생성물 1

HCID 193501462,3-dimethylbenzo(B)phenazine

시약·촉매·용매 2

HCID 176Acetic Acid용매
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 702
Ethanol
용매

실험 절차

The 2,3-dimethylbenzo(B)phenazine was prepared by the condensation of 2,3-diaminonapthalene with 4,5-dimethyl-1,2-benzoquinone in 4:1 ethanol to acetic acid at reflux for 2 hours. The phenazine was alkylated by the procedure of Synthesis Example 8, using iodomethane. Electrochemical analysis was consistent with an N,N'-dialkylated phenazine.

후처리

  1. temperatureat reflux for 2 hours

출처 및 근거

ORD 기록
ord-38d5154dd9e94c729f7719601216679e
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05998617

반응 노트

불러오는 중…