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Hydrazine hydrate (1:1) → 4-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazide

HRID 473932
ノート
印刷プレビュー

反応式

HRID 473932 の反応式
CN(C(O[N:9]1[N:17]=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[OH:23][C:24]([CH3:51])([CH3:50])[CH2:25][C@@:26]1([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[O:31][C:30](=[O:32])[N:29]([C@H:33]([C:35]2[CH:43]=[CH:42][C:38]([C:39](O)=[O:40])=[CH:37][CH:36]=2)[CH3:34])[CH2:28][CH2:27]1.C(N(C(C)C)C(C)C)C.O.NN>CN(C)C=O.O>[OH:23][C:24]([CH3:51])([CH3:50])[CH2:25][C@@:26]1([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[O:31][C:30](=[O:32])[N:29]([C@H:33]([C:35]2[CH:43]=[CH:42][C:38]([C:39]([NH:9][NH2:17])=[O:40])=[CH:37][CH:36]=2)[CH3:34])[CH2:28][CH2:27]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 24654Hydrazine hydrate (1:1)HCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 581092884-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid

生成物 1

HCID 668580744-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazide

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

TBTU [2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate, 0.33 g] was added to 4-{(S)-1-[(S)-6-(2-hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid (0.37 g) and EtNiPr2 (0.41 mL) dissolved in dimethylformamide (5 mL). After stirring the solution at room temperature for 10 min, hydrazine hydrate (0.23 mL) was added. The solution was stirred at room temperature overnight and then diluted with water. The resulting mixture was extracted with ethyl acetate and the combined extracts were washed with brine and dried (MgSO4). The solvent was removed and the residue was purified by chromatography on silica gel (CH2Cl2/MeOH 98:2->90:10) to afford the title compound as a colorless foam-like solid.

後処理

  1. stirringThe solution was stirred at room temperature overnight
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. washthe combined extracts were washed with brine
  4. dry with materialdried (MgSO4)
  5. customThe solvent was removed
  6. customthe residue was purified by chromatography on silica gel (CH2Cl2/MeOH 98:2->90:10)

出典と根拠

ORDレコード
ord-6f86fa678ab74a7491ca3faad95f69b2
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637505B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート