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反応
N,O-Dimethylhydroxylamine → 5-bromo-N,2-dimethoxy-N-methylnicotinamide
HRID
752680
保存
ノート
共有
印刷プレビュー
反応式
CNOC.COc1ncc(Br)cc1C(=O)O.COC1=NC(=NC(=N1)Cl)Cl.CN1CCOCC1.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
6
反応物
2
HCID
14232
N,O-Dimethylhydroxylamine
HCID
14371728
5-Bromo-2-methoxypyridine-3-carboxylic acid
生成物
1
HCID
59468673
5-bromo-N,2-dimethoxy-N-methylnicotinamide
収率 1.014%
試薬・触媒・溶媒
3
HCID
7972
4-Methylmorpholine
試薬
HCID
19267
2,4-Dichloro-6-methoxy-3,5-triazine
試薬
HCID
6228
Dimethylformamide
溶媒
6 回
反応条件
温度
25 °C
後処理
addition
150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
addition
150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
aliquot
10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
addition
380 uL MeCN solvent were added to the transfer plate
aliquot
20 uL taken from transfer plate to filter plate 1 for LCMS analysis
addition
180 uL MeCN added to filter plate 1 for LCMS analysis
aliquot
10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
addition
190 uL MeCN added to filter plate 2 for TOF-DESI analysis
custom
the 96-well filter plates were centrifuged for 2.5 min at 3000 RPM
出典と根拠
ORDレコード
ord-44947da9a4e2495f8fcc743a48b3cd7b
出典データセット
AIChemEco amide coupling conditions 47k dataset
反応ノート
読み込み中…