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4-Methylmorpholine → HCID 22719739、化合物

HRID 1582069
ノート
印刷プレビュー

反応式

HRID 1582069 の反応式
Cl.[CH3:2][N:3](C)[CH2:4][CH2:5][CH2:6][N:7]=C=NCC.O.ON1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2N=N1.CN1CC[O:28]CC1.[CH2:31]([O:38][C:39]([CH:41]([CH2:51][CH2:52][C:53]1[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1)[CH2:42][C:43]1([C:48]([OH:50])=O)[CH2:47][CH2:46][CH2:45][CH2:44]1)=[O:40])C1C=CC=CC=1>CN(C)C=O>[CH3:2][NH:3][C:4](=[O:28])[CH2:5][CH2:6][NH:7][C:48]([C:43]1([CH2:42][CH:41]([CH2:51][CH2:52][C:53]2[CH:54]=[CH:55][CH:56]=[CH:57][CH:58]=2)[C:39]([O:38][CH2:31][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:40])[CH2:44][CH2:45][CH2:46][CH2:47]1)=[O:50]
参加物反応条件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 79724-MethylmorpholineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 22719740HCID 22719740、化合物

生成物 1

HCID 22719739HCID 22719739、化合物

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

反応条件

温度
90 °C

実験手順

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (122 mg, 0.64 mmol), 1-hydroxybenzotriazole hydrate (86 mg, 0.64 mmol) and 4-methylmorpholine (173 μl, 1.59 mmol) were added sequentially to a cooled solution of 1-{2-[(benzyloxy)carbonyl]4-phenylbutyl}cyclopentane-carboxylic acid (EP 274234) (202 mg, 0.53 mmol) in N,N-dimethylformamide (5 ml) at room temperature, followed by the amine hydrochloride from preparation 6 (6/23) (146 mg, 1.06 mmol), and the reaction stirred at 90° C. for 18 hours. The cooled solution was concentrated under reduced pressure and the residue partitioned between water (20 ml) and ethyl acetate (100 ml). The layers were separated, the organic phase washed with water (3×30 ml), brine (25 ml) dried (MgSO4), and evaporated under reduced pressure to give a clear oil. The crude product was purified by column chromatography on silica gel using dichloromethane:methanol (98:2) as eluant to afford the title compound as a colourless oil, 162 mg, 67%; 1H NMR (CDCl3, 400 MHz) δ: 1.38-1.53 (m, 2H), 1.53-1.96 (m, 8H), 2.02 (m, 2H), 2.27 (t, 2H), 2.46 (m, 3H), 2.76 (d, 3H), 3.44 (m, 2H), 5.13 (s, 2H), 5.79 (bs, 1H), 6.38 (m, 1H), 7.06 (d, 2H), 7.18 (m, 1H), 7.22 (m, 2H), 7.38 (m, 5H); LRMS: m/z 465.5 (MH+).

後処理

  1. concentrationThe cooled solution was concentrated under reduced pressure
  2. customthe residue partitioned between water (20 ml) and ethyl acetate (100 ml)
  3. customThe layers were separated
  4. washthe organic phase washed with water (3×30 ml), brine (25 ml)
  5. dry with materialdried (MgSO4)
  6. customevaporated under reduced pressure
  7. customto give a clear oil
  8. customThe crude product was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-3886bc4340a545a88a19d7b9b1ac2ee3
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06734186B1

反応ノート

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