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Diisopropylethylamine → HCID 59619453、化合物

HRID 1367514
ノート
印刷プレビュー

反応式

HRID 1367514 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C@@H:11]2[CH2:15][C@@H:14]([C:16](O)=[O:17])[C@H:13]([C:19]([N:21]3[CH2:24][C:23]([F:26])([F:25])[CH2:22]3)=[O:20])[CH2:12]2)(=[O:10])=[O:9])=[C:4]([C:27]([F:30])([F:29])[F:28])[CH:3]=1.C(N(CC)C(C)C)(C)C.C[NH3+].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)[C:53]2[N:54]=C[CH:56]=[CH:57][C:52]=2[N:51]=N1.F[P-](F)(F)(F)(F)F.C1C(N)(C#N)C1.Cl>C(#N)C>[C:53]([C:52]1([NH:51][C:16]([C@@H:14]2[CH2:15][C@@H:11]([S:8]([C:5]3[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=3[C:27]([F:29])([F:30])[F:28])(=[O:10])=[O:9])[CH2:12][C@H:13]2[C:19]([N:21]2[CH2:22][C:23]([F:25])([F:26])[CH2:24]2)=[O:20])=[O:17])[CH2:56][CH2:57]1)#[N:54]
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 145863631-Amino-1-cyclopropanecarbonitrile hydrochlorideHCID 866211442-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate MethanaminiumHCID 86649026HCID 86649026、化合物

生成物 1

HCID 59619453HCID 59619453、化合物収率 85%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a mixture of (1R,2R,4S)-4-(4-Bromo-2-trifluoromethyl-benzenesulfonyl)-2-(3,3-difluoro-azetidine-1-carbonyl)-cyclopentanecarboxylic acid (150 mg, 0.29 mmol), N,N-diisopropylethylamine (0.15 mL, 0.87 mmol), 2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate methanaminium (221 mg, 0.58 mmol) in acetonitrile was added 1-amino-cyclopropyl cyanic hydrochloride (41 mg, 0.34 mmol). The reaction mixture was stirred at room temperature for 16 h then concentrated in vacuo and partitioned between ethyl acetate and an aqueous solution of sodium carbonate (5% w/w). The aqueous layer was extracted with ethyl acetate then the combined organic layers were washed with aqueous hydrochloric acid (1N) and brine then dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel with a gradient of dichloromethane/methanol (98:2 v/v) as eluant to afford the title compound (144 mg, 85%) as a brown solid. MS (EI): 584.0 (M−H)−.

後処理

  1. concentrationthen concentrated in vacuo
  2. custompartitioned between ethyl acetate
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. washthe combined organic layers were washed with aqueous hydrochloric acid (1N) and brine
  5. dry with materialthen dried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography on silica gel with a gradient of dichloromethane/methanol (98:2 v/v) as eluant

出典と根拠

ORDレコード
ord-709e4a2601904c6bb3ed54a1625e74b0
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07893099B2

反応ノート

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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