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Hydrochloric Acid → HCID 178524916、化合物

HRID 1874849
ノート
印刷プレビュー

反応式

HRID 1874849 の反応式
[Cl:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[C:7]([O:9]C)=[O:8].CO.[OH-].[Na+].Cl>O1CCOCC1>[Cl:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[C:7]([OH:9])=[O:8]
参加物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 313Hydrochloric AcidHCID 887MethanolHCID 14798Sodium HydroxideHCID 178499148HCID 178499148、化合物

生成物 1

HCID 178524916HCID 178524916、化合物収率 94%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A solution of methyl 4-chloro-1H-imidazole-5-carboxylate (0.061 g, 0.4 mmol) was stirred in a solution of MeOH (2 mL), dioxane (2 mL) and 2N NaOH (1.9 mL, 3.8 mmol) at RT for 4 days. The reaction mixture was then acidified by addition of 1M HCl (20 mL) and extracted with EtOAc. The organic extracts were dried (Na2SO4), and the solvent was evaporated to provide 4-chloro-1H-imidazole-5-carboxylic acid (0.0523 g, 94%) as a white solid which was used without further purification. 4-Chloro-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-imidazole-5-carboxamide was prepared in a similar manner as described herein from 3-{[3-aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.054 g, 0.17 mmol), 4-chloro-1H-imidazole-5-carboxylic acid (0.026 g, 0.17 mmol), HATU (0.086 g, 0.23 mmol), DIPEA (0.039 mL, 0.23 mmol) and DMF (2 mL). Purification was accomplished by Reverse-Phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.008 g, 10%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 13.16 (br. s., 1H), 8.24 (br. s., 1H), 7.82 (s, 1H), 7.78 (s, 1H), 7.45-7.54 (m, 3H), 7.35-7.42 (m, 1H), 4.54 (s, 2H). ES-LCMS: m/z 439.0, 441.0 (M+1).

後処理

  1. extractionextracted with EtOAc
  2. dry with materialThe organic extracts were dried (Na2SO4)
  3. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-941543498c1d43e4a67a2bb4850a4005
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08304419B2

反応ノート

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