Dimethylformamide → HCID 69892327、化合物

HRID 1265496ノート

反応式

HRID 1265496 の反応式
[C:1]([O:5][C:6](NC1C=C(C(O)=O)N(C)C=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:18]([O:27][C:28](=[O:37])[C:29]1[CH:34]=[CH:33][C:32]([CH2:35]Br)=[CH:31][CH:30]=1)[C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:20].C([N:41]([CH:44]([CH3:46])C)[CH2:42][CH3:43])(C)C.CN(C=[O:51])C>>[CH2:18]([O:27][C:28](=[O:37])[C:29]1[CH:34]=[CH:33][C:32]([CH2:35][O:51][C:44]2[NH:41][CH:42]=[CH:43][CH:46]=2)=[CH:31][C:30]=1[C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:20]

参加物

5

実験手順

A solution of Boc-pyrrole-OH (8)(2.9 g 12 mmol), 4-(bromomethyl)benzoic acid phenacyl ester (22) (4 g, 12 mmol) and diisopropylethylamine (3.0 ml, 16.8 mmol) in 60 ml of DMF were stirred at 50° C. for 6 hours. The solution was cooled and partitioned between 400 ml of water and 400 ml of ethyl ether. The ether layer was washed with (2×200 ml each) of 10% citric acid, brine. saturated sodium bicarbonate and brine. The organic phase was dried with sodium sulfate and concentrated in vacuo to yield compound 38 as light white foam which was used without further purification (5.4 g, 97% yield). TLC (2:3 hexane/ethyl acetate) Rf 0.6; 1H NMR (DMSO-d6) δ9.14 (s, 1H), 8.03 (m, 4H), 7.67 (m, 1H), 7.55 (m, 4H), 7.13 (s, 1H), 6.72 (d, 1H, J=1.5 Hz), 5.74 (s, 1H), 5.32 (s, 1H), 3.79 (s, 3H), 1.42 (s, 9H); 13C NMR (DMSO-d6) δ193.2, 165.5, 160.4, 153.2, 143.1, 134.5, 130.1, 129.5, 128.3, 128.2, 123.8, 120.3, 118.8, 108.2, 79.1, 67.7, 64.6, 36.7,28.6.

後処理

  1. temperatureThe solution was cooled
  2. custompartitioned between 400 ml of water and 400 ml of ethyl ether
  3. washThe ether layer was washed with (2×200 ml each) of 10% citric acid, brine
  4. dry with materialThe organic phase was dried with sodium sulfate
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ea5eec8a4362425dbf8f7b93a38f7570
出典データセット
uspto-grants-2003_04
特許番号
US06545162B1

反応ノート

読み込み中…