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Sodium Methoxide → HCID 178453509、化合物

HRID 717740
ノート
印刷プレビュー

反応式

HRID 717740 の反応式
C[O:2][C:3](=O)[C:4]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:16][CH2:17][CH2:18][NH:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])=[CH:10][CH:9]=1)=[CH:5]OC.[Br:35][C:36]1[CH:41]=[CH:40][C:39]([C:42]2[NH:46][C:45]([NH2:47])=[N:44][CH:43]=2)=[CH:38][CH:37]=1.C[O-].[Na+]>C(O)C>[C:30]([O:29][C:27](=[O:28])[N:15]([CH2:14][C:11]1[CH:12]=[CH:13][C:8]([C:4]2[C:3](=[O:2])[N:47]=[C:45]3[NH:46][C:42]([C:39]4[CH:38]=[CH:37][C:36]([Br:35])=[CH:41][CH:40]=4)=[CH:43][N:44]3[CH:5]=2)=[CH:9][CH:10]=1)[CH2:16][CH2:17][CH2:18][NH:19][C:20]([O:22][C:23]([CH3:25])([CH3:26])[CH3:24])=[O:21])([CH3:32])([CH3:31])[CH3:33]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10942334Sodium Methoxide2 回HCID 130122555-(4-bromophenyl)-1H-imidazol-2-amineHCID 665788052-(4-{[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-methyl}-phenyl)-3-methoxy-acrylic acid methyl ester

生成物 1

HCID 178453509HCID 178453509、化合物収率 52.1%

試薬・触媒・溶媒 1

HCID 702
Ethanol
溶媒

実験手順

To a mixture of 2-(4-{[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-methyl}-phenyl)-3-methoxy-acrylic acid methyl ester (5.70 g, 11.92 mmol), 5-(4-bromo-phenyl)-1H-imidazol-2-ylamine (2.84 g, 11.92 mmol) and ethanol (60 mL) was added a solution of sodium methoxide (12 mL, 0.5 M in methanol, 6 mmol). The resulted mixture was refluxed for 18 h, additional 12 mL of sodium methoxide (0.5 M in methanol, 6 mmol) was added and continued to reflex for 20 h. The reaction was concentrated and diluted with EtOAc (300 mL) and washed with water (200 mL), brine (200 mL). The EtOAc solution was concentrated. The crude product was purified by flash chromatography (0%-8% Methanol in dichloromethane) to give desired product (4.05 g, 52%) as brown solid. 1NMR (300 MHz, CDCl3): δ 7.96 (s, 1H), 7.68 (d, J=8.1 Hz, 2H), 7.54 (m, 2H), 7.35(s, 1H), 7.27 (d, J=8.1 Hz, 2H), 5.25 (br.s, 0.5H), 4.70 (br.s, 0.5H), 4.44 (s, 2H), 3.29 (m, 2H), 3.11 (m, 2H), 1.67 (m, 2H), 1.52 (br.d, 9H), 1.44 (s, 9H). LCMS (EI) m/z: 654 (M+H+).

後処理

  1. temperatureThe resulted mixture was refluxed for 18 h
  2. concentrationThe reaction was concentrated
  3. additiondiluted with EtOAc (300 mL)
  4. washwashed with water (200 mL), brine (200 mL)
  5. concentrationThe EtOAc solution was concentrated
  6. customThe crude product was purified by flash chromatography (0%-8% Methanol in dichloromethane)

出典と根拠

ORDレコード
ord-c658ce91915146a5b9844e4e7bcf37e8
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09193731B2

反応ノート

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