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1-Hydroxybenzotriazole → diethyl 2-(3,4-dimethyl-benzyl)-2-{2-oxo-2-[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-ethyl}-malonate

HRID 644366
ノート
印刷プレビュー

反応式

HRID 644366 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([C:20]([O:22][CH2:23][CH3:24])=[O:21])([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:11][C:12](O)=[O:13])[CH:5]=[CH:6][C:7]=1[CH3:8].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N(O)N=NC=2C=1.C(N(C(C)C)C(C)C)C.[NH:66]1[CH2:71][CH2:70][CH:69]([N:72]2[CH2:81][C:80]3[C:75](=[CH:76][CH:77]=[CH:78][CH:79]=3)[NH:74][C:73]2=[O:82])[CH2:68][CH2:67]1>O.C1COCC1>[CH3:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[CH3:8])[CH2:9][C:10]([CH2:11][C:12](=[O:13])[N:66]1[CH2:67][CH2:68][CH:69]([N:72]2[CH2:81][C:80]3[C:75](=[CH:76][CH:77]=[CH:78][CH:79]=3)[NH:74][C:73]2=[O:82])[CH2:70][CH2:71]1)([C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:15]([O:17][CH2:18][CH3:19])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 110425973-(Piperidin-4-yl)-3,4-dihydroquinazolin-2(1H)-oneHCID 685789934-(3,4-Dimethyl-phenyl)-3,3-bis-ethoxycarbonyl-butanoic acid

生成物 1

HCID 68579159
diethyl 2-(3,4-dimethyl-benzyl)-2-{2-oxo-2-[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-ethyl}-malonate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 10.0 g (29.7 mmol) 4-(3,4-dimethyl-phenyl)-3,3-bis-ethoxycarbonyl-butanoic acid, 10.5 g (32.7 mmol) TBTU, 4.2 g (30.5 mmol) HOBt, 5.8 mL (32.4 mmol) ethyldiisopropylamine, 270 mL THF and 30 mL water was stirred for 15 min at RT and then combined with 7.6 g (32.9 mmol) 3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one. The reaction mixture was stirred for 5 h at RT and evaporated down under reduced pressure. The residue was stirred with 150 mL saturated NaHCO3 solution, suction filtered, washed with water and dried in the circulating air dryer.

後処理

  1. stirringThe reaction mixture was stirred for 5 h at RT
  2. customevaporated down under reduced pressure
  3. stirringThe residue was stirred with 150 mL saturated NaHCO3 solution, suction
  4. filtrationfiltered
  5. washwashed with water
  6. customdried in the circulating air dryer

出典と根拠

ORDレコード
ord-85f96a28cc34453486f7c8f4b29cfde3
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07700589B2

反応ノート

読み込み中…

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