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

Diacetoxyiodosobenzene → 6-Oxo-1,6-dihydro-[1,2,4]triazine-5-carboxylic acid ethyl ester

HRID 2076828
노트
인쇄 미리보기

반응식

HRID 2076828 반응식
[CH2:1]([O:3][C:4]([CH:6]1[C:11](=[O:12])[NH:10][N:9]=[CH:8][NH:7]1)=[O:5])[CH3:2].C(OC1C(OC(=O)C)=C(I=O)C=CC=1)(=O)C>C(O)C>[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[NH:10][N:9]=[CH:8][N:7]=1)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21113495DiacetoxyiodosobenzeneHCID 178470304HCID 178470304, 화합물

생성물 1

HCID 117152386-Oxo-1,6-dihydro-[1,2,4]triazine-5-carboxylic acid ethyl ester수율 64.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

6-Oxo-1,4,5,6-tetrahydro-[1,2,4]triazine-5-carboxylic acid ethyl ester (329 mg, 1.92 mmol) was dissolved in ethanol (9 ml) and diacetoxyiodosobenzene (644 mg, 1.99 mmol) was added in one portion. After 2 h at ambient temperature all volatiles were removed and the remaining residue was purified by column chromatography (silica gel, heptane/ethyl acetate 70:30 to 50:50) to give the title compound (209 mg, 1.24 mmol; 64%) as yellow solid. MS: m/e=170.1 [M+H+].

후처리

  1. customAfter 2 h at ambient temperature all volatiles were removed
  2. customthe remaining residue was purified by column chromatography (silica gel, heptane/ethyl acetate 70:30 to 50:50)

출처 및 근거

ORD 기록
ord-8ad4d04b8400455e8a23b1a75102ad92
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928106B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트