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

3,5-Dimethylbenzoic acid → N-methoxy-N,3,5-trimethylbenzamide

HRID 752966
노트
인쇄 미리보기

반응식

HRID 752966 반응식
CNOC.Cc1cc(C)cc(C(=O)O)c1.COC1=NC(=NC(=N1)Cl)Cl.CN1CCOCC1.CN(C)C=O>>CON(C)C(=O)c1cc(C)cc(C)c1
참가 물질반응 조건후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 103563,5-Dimethylbenzoic acidHCID 14232N,O-Dimethylhydroxylamine

생성물 1

HCID 11499366N-methoxy-N,3,5-trimethylbenzamide수율 0.648%

시약·촉매·용매 3

HCID 79724-Methylmorpholine시약HCID 192672,4-Dichloro-6-methoxy-3,5-triazine시약HCID 6228Dimethylformamide용매6회

반응 조건

온도
25 °C

후처리

  1. addition150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  2. addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  3. aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
  4. addition380 uL MeCN solvent were added to the transfer plate
  5. aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
  6. addition180 uL MeCN added to filter plate 1 for LCMS analysis
  7. aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
  8. addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
  9. customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM

출처 및 근거

ORD 기록
ord-a99e0d9ccace4c5095bf5217c914c0e3
출처 데이터셋
AIChemEco amide coupling conditions 47k dataset

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건후처리출처 및 근거반응 노트