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Hydrochloric Acid → (4-Benzyloxy-phenyl)-(-6-(3-methylisoxazol-5-yl)-quinazolin-4-yl)-amine hydrochloride

HRID 2306737
ノート
印刷プレビュー

反応式

HRID 2306737 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([NH:15][C:16]2[C:25]3[C:20](=[CH:21][CH:22]=[C:23]([C:26]#[CH:27])[CH:24]=3)[N:19]=[CH:18][N:17]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:28]([CH2:31][CH3:32])([O-])=[O:29].C1(N=C=O)C=CC=CC=1.[ClH:42]>C(N(CC)CC)C.C(OCC)(=O)C.ClCCl>[ClH:42].[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([NH:15][C:16]2[C:25]3[C:20](=[CH:21][CH:22]=[C:23]([C:26]4[O:29][N:28]=[C:31]([CH3:32])[CH:27]=4)[CH:24]=3)[N:19]=[CH:18][N:17]=2)=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 6587NitroethaneHCID 7672Phenyl isocyanateHCID 22609768(4-Benzyloxy-phenyl)(6-ethynylquinazolin-4-yl)-amine

生成物 1

HCID 22609788(4-Benzyloxy-phenyl)-(-6-(3-methylisoxazol-5-yl)-quinazolin-4-yl)-amine hydrochloride収率 11%

試薬・触媒・溶媒 3

HCID 8471
Triethylamine
触媒
HCID 6344Dichloromethane溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A stirred mixture of (4-benzyloxy-phenyl)-(6-ethynylquinazolin-4-yl)-amine (0.20 g, 0.57 mmol), nitroethane (0.20 g, 2.7 mmol), phenylisocyanate (0.15 ml , 0.164 g, 1.38 mmol), and triethylamine (3 drops) in a mixture of ethyl acetate (10 ml) and dichloromethane (5 ml) was heated at reflux for 18 hours. After cooling the mixture was filtered to remove solid, and the concentrated filtrate was purified by silica gel chromatography, eluting with 50% ethyl acetate/i-hexane. After concentration of the appropriate fractions, the material obtained was treated with methanolic HCl, the solvent was removed in vacuo and the residue was triturated with ether to give the title compound as a yellow solid (0.027 g, 0.061 mmol, 11%); δH [2H6]DMSO 12.0 (1H, s), 9.55 (1H, s), 8.91 (1H, s), 8.48 (1H, d), 8.03 (1H, d), 7.68 (2H, d), 7.32-7.55 (5H, m), 7.22 (1H, s), 7.15 (2H, d), 5.18 (2H, s), 2.35 (3H, s); m/z (M+1+) 409.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 18 hours
  3. temperatureAfter cooling the mixture
  4. filtrationwas filtered
  5. customto remove solid
  6. customthe concentrated filtrate was purified by silica gel chromatography
  7. washeluting with 50% ethyl acetate/i-hexane
  8. customAfter concentration of the appropriate fractions, the material obtained
  9. customthe solvent was removed in vacuo
  10. customthe residue was triturated with ether

出典と根拠

ORDレコード
ord-a04e9c4bf03148e58a6760def47031fe
出典データセット
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06828320B2

反応ノート

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