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Sodium cyanoborohydride → 1-[2-(4-Nitrophenyl)ethyl]-4-{2-[4-nitro-3-(trifluoromethyl)phenyl]ethyl}piperazin-2-one

HRID 1466119
ノート
印刷プレビュー

反応式

HRID 1466119 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH:11]=O)=[CH:6][C:5]=1[C:13]([F:16])([F:15])[F:14])([O-:3])=[O:2].[N+:17]([C:20]1[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][N:28]2[CH2:33][CH2:32][NH:31][CH2:30][C:29]2=[O:34])=[CH:22][CH:21]=1)([O-:19])=[O:18].C([BH3-])#N.[Na+]>CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].C(O)C>[N+:17]([C:20]1[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][N:28]2[CH2:33][CH2:32][N:31]([CH2:11][CH2:10][C:7]3[CH:8]=[CH:9][C:4]([N+:1]([O-:3])=[O:2])=[C:5]([C:13]([F:16])([F:15])[F:14])[CH:6]=3)[CH2:30][C:29]2=[O:34])=[CH:22][CH:21]=1)([O-:19])=[O:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 5003444Sodium cyanoborohydrideHCID 89524879[4-Nitro-3-(trifluoromethyl)phenyl]acetaldehydeHCID 895248911-[2-(4-Nitrophenyl)ethyl]piperazin-2-one

生成物 1

HCID 895335101-[2-(4-Nitrophenyl)ethyl]-4-{2-[4-nitro-3-(trifluoromethyl)phenyl]ethyl}piperazin-2-one

試薬・触媒・溶媒 2

HCID 11026Titanium isopropoxide触媒
HCID 702Ethanol溶媒

実験手順

A solution of 1-nitro-4-(prop-2-en-1-yl)-2-(trifluoromethyl)benzene in methanol and cooled to −78° C. Ozone was bubbled through the solution until it turned blue. Excess ozone was removed by bubbling nitrogen through the solution, followed by addition of triphenylphosphine (1.1 g, 4.3 mmol). The mixture was warmed up naturally. TLC showed formation of the desired product. The crude material was adsorbed onto silica gel, and purified by flash chromatography to afford the desired [4-nitro-3-(trifluoromethyl)phenyl]acetaldehyde. The aldehyde (20 mg, 0.070 mmol) was treated with 1-[2-(4-nitrophenyl)ethyl]piperazin-2-one (16 mg, 0.070 mmol) and titanium(IV) isopropoxide (0.20 mL). After stirring the mixture for 15 minutes, ethanol (2 mL) and sodium cyanoborohydride (44 mg, 0.70 mmol) was added into the reaction. The mixture was allowed to stir for 4 hours. LC showed formation of the desired product. The reaction was diluted with ethyl acetate, washed with brine, dried over sodium sulfate, and concentrated to give the crude product. The crude product was purified by mass-directed reverse phase HPLC (AcCN-Water with 0.1% TFA). LC-MS (IE, m/z): 467 [M+1]+.

後処理

  1. stirringto stir for 4 hours

出典と根拠

ORDレコード
ord-0ee1b14967644b409bdb7f1b86df1301
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999990B2

反応ノート

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