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Triethylamine → 8,9-Dimethoxy-1-nitro-5-[2-(N,N-dimethylamino)ethyl]-5H-dibenzo[c,h][1,6]naphthyridin-6-one

HRID 1612036
ノート
印刷プレビュー

反応式

HRID 1612036 の反応式
[N+:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[N:12]=[CH:11][CH:10]=[C:9]2[N:14]([CH2:28][CH2:29][N:30]([CH3:32])[CH3:31])[C:15](=[O:27])[C:16]1[C:21](OC)=[C:20]([O:24][CH3:25])[CH:19]=[CH:18][C:17]=1I)([O-:3])=[O:2].C(Cl)(=O)[C:34](Cl)=[O:35].COC1C=C(C(I)=CC=1OC)C(O)=O.[N+](C1C=CC=C2C=1N=CC=C2NCCN(C)C)([O-])=O.C(N(CC)CC)C>C(Cl)Cl>[CH3:25][O:24][C:20]1[C:19]([O:35][CH3:34])=[CH:18][C:17]2[C:10]3[C:9](=[C:8]4[CH:7]=[CH:6][CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[C:13]4=[N:12][CH:11]=3)[N:14]([CH2:28][CH2:29][N:30]([CH3:32])[CH3:31])[C:15](=[O:27])[C:16]=2[CH:21]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 27584222-Iodo-4,5-dimethoxybenzoic acidHCID 22252603N'-(8-Nitroquinolin-4-yl)-N,N-dimethylethane-1,2-diamineHCID 69236752N-(8-Nitroquinolin-4-yl)-N-(N,N-dimethylaminoethyl)-2-iodo-5,6-dimethoxybenzamide

生成物 1

HCID 10025241
8,9-Dimethoxy-1-nitro-5-[2-(N,N-dimethylamino)ethyl]-5H-dibenzo[c,h][1,6]naphthyridin-6-one
収率 85%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

N-(8-Nitroquinolin-4-yl)-N-(N,N-dimethylaminoethyl)-2-iodo-5,6-dimethoxybenzamide (8a). Oxalyl chloride (762 mg, 6.0 mmol) was added to a solution of 3,4-dimethoxy-6-iodobenzoic acid (570 mg, 1.85 mmol) in anhydrous methylene chloride (20 mL), and the stirred mixture was refluxed for 3 hours. The mixture was then concentrated to dryness under reduced pressure. The acid chloride was redissolved in 20 mL of anhydrous methylene chloride, and this solution was added to a solution of 7a (400 mg, 1.54 mmol) and triethylamine (1.14 g, 11.3 mmol) in methylene chloride (20 mL), and the resulting mixture was stirred at reflux overnight. The reaction mix was cooled and washed with saturated sodium bicarbonate (3×75 mL), and extracted with 5% aqueous HCl (4×100 mL). The combined aqueous extracts were basified with 30% NaOH and then extracted with chloroform (3×100 mL). Combined organic extracts were then dried (MgSO4) and evaporated to give 722 mg of the amide, in 85% yield; 1H NMR (CDCl3) δ 2.30 (s, 6H), 2.69 (m, 2H), 3.32 (s, 3H), 3.74 (s, 3H), 3.95 (m, 1H), 4.57 (m, 1H), 6.41 (s, 1H), 7.02 (s, 1H), 7.75 (m, 2H), 8.05 (d, 1H, J=6.6), 8.44 (d, 1H, J=8.4), 8.95 (d, 1H, J=4.4); 13C NMR (CDCl3) δ 45.4, 47.3, 55.7, 56.1, 56.5, 82.7, 110.7, 121.9, 123.3, 124.0, 126.1, 126.9, 127.2, 133.1, 140.9, 147.4, 148.4, 149.0, 150.1, 153.0, 169.9; IR (CHCl3) 1362, 1536, 1655.

後処理

  1. temperaturethe stirred mixture was refluxed for 3 hours
  2. concentrationThe mixture was then concentrated to dryness under reduced pressure
  3. dissolutionThe acid chloride was redissolved in 20 mL of anhydrous methylene chloride
  4. temperatureat reflux overnight
  5. additionThe reaction mix
  6. temperaturewas cooled
  7. washwashed with saturated sodium bicarbonate (3×75 mL)
  8. extractionextracted with 5% aqueous HCl (4×100 mL)
  9. extractionextracted with chloroform (3×100 mL)
  10. dry with materialCombined organic extracts were then dried (MgSO4)
  11. customevaporated

出典と根拠

ORDレコード
ord-6edd3000e9ad4e6ab3687fb7d5cdb03f
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06992089B2

反応ノート

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