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Diisopropylethylamine → HCID 15895101、化合物

HRID 1953045
ノート
印刷プレビュー

反応式

HRID 1953045 の反応式
[C:1]([O:5][C:6]([N:8]1[C:12](=[O:13])[C@H:11]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[CH2:10][C@@H:9]1[C:22](O)=[O:23])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N([CH:31]([CH3:33])[CH3:32])CC)(C)C.Cl.[CH2:35]([O:42][NH2:43])C1C=CC=CC=1.B(F)([O-])[O-].B(F)([O-])[O-].B(F)([O-])[O-].B(F)([O-])[O-].B(F)([O-])[O-].B(F)([O-])[O-].N1(O[P+](N(C)C)(N(C)C)N(C)C)[C:72]2C=CC=[CH:76][C:71]=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>C(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[C@@H:9]([C:22](=[O:23])[NH:43][O:42][CH2:35][C:32]2[CH:31]=[CH:33][CH:76]=[CH:71][CH:72]=2)[CH2:10][C@@H:11]([C:14]2[CH:15]=[CH:16][C:17]([O:20][CH3:21])=[CH:18][CH:19]=2)[C:12]1=[O:13])=[O:7])([CH3:2])([CH3:4])[CH3:3]
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 4

HCID 81531DiisopropylethylamineHCID 102312Benzyloxyamine hydrochlorideHCID 10735516HCID 10735516、化合物HCID 86755729HCID 86755729、化合物

生成物 1

HCID 15895101HCID 15895101、化合物

試薬・触媒・溶媒

1
HCID 6344Dichloromethane溶媒

実験手順

To a solution of (2R, 4S)-4-(4-methoxyphenyl)-5-oxopyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (305 mg, 0.91 mmol), diisopropylethylamine (0.35 mL, 2.0 mmol) and O-benzylhydroxylamine hydrochloride (160 mg, 1.0 mmol) in methylene chloride (20 mL) was added (benztriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluoroborate (443 mg, 1.0 mmol). The reaction was stirred at room temperature overnight. After dilution with methylene chloride, the mixture was washed with aqueous saturated sodium bicarbonate solution, water and brine. The solution was dried over magnesium sulfate and concentrated to a white solid from which the title compound (294 mg, 73%) was isolated by flash chromatography eluting with 25% hexane in ethyl acetate.

後処理

  1. washAfter dilution with methylene chloride, the mixture was washed with aqueous saturated sodium bicarbonate solution, water and brine
  2. dry with materialThe solution was dried over magnesium sulfate
  3. concentrationconcentrated to a white solid from which the title compound (294 mg, 73%)
  4. customwas isolated by flash chromatography
  5. washeluting with 25% hexane in ethyl acetate

出典と根拠

ORDレコード
ord-946b03de09e2416d95578084d658a897
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06114361

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