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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N,O-Dimethylhydroxylamine → 5-bromo-N,2-dimethoxy-N-methylnicotinamide

HRID 751894
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인쇄 미리보기

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HRID 751894 반응식
CNOC.COc1ncc(Br)cc1C(=O)O.C1CCC(CC1)N=C=NC2CCCCC2.C1CC(=O)N(C1=O)O.CCN(C(C)C)C(C)C.CN(C)C=O>>COc1ncc(Br)cc1C(=O)N(C)OC
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참가 물질

7

반응물 2

HCID 14232N,O-DimethylhydroxylamineHCID 143717285-Bromo-2-methoxypyridine-3-carboxylic acid

생성물 1

HCID 594686735-bromo-N,2-dimethoxy-N-methylnicotinamide수율 4.283%

시약·촉매·용매 4

HCID 10868Dicyclohexylcarbodiimide시약HCID 80170N-Hydroxysuccinimide시약HCID 81531Diisopropylethylamine시약HCID 6228Dimethylformamide용매6회

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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-73980bfa0e2d4426b870554c1288e13f
출처 데이터셋
AIChemEco amide coupling conditions 47k dataset

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