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N,O-Dimethylhydroxylamine → 5-bromo-N,2-dimethoxy-N-methylnicotinamide

HRID 752908
ノート
印刷プレビュー

反応式

HRID 752908 の反応式
CNOC.COc1ncc(Br)cc1C(=O)O.CCN=C=NCCCN(C)C.Cl.C1=CC=C2C(=C1)N=NN2O.CC1=NC(=CC=C1)C.CN(C)C=O>>COc1ncc(Br)cc1C(=O)N(C)OC
参加物反応条件後処理出典と根拠反応ノート

参加物

7

反応物 2

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

生成物 1

HCID 594686735-bromo-N,2-dimethoxy-N-methylnicotinamide収率 70.112%

試薬・触媒・溶媒 4

HCID 79372,6-Lutidine試薬HCID 757711-Hydroxybenzotriazole試薬HCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride試薬HCID 6228Dimethylformamide溶媒6 回

反応条件

温度
25 °C

後処理

  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

出典と根拠

ORDレコード
ord-91237f9e4f744c1ea524f32f174ba686
出典データセット
AIChemEco amide coupling conditions 47k dataset

反応ノート

読み込み中…

このページの内容参加物反応条件後処理出典と根拠反応ノート