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Cyanamide → HCID 25140759、化合物

HRID 1669145
ノート
印刷プレビュー

反応式

HRID 1669145 の反応式
[N+:1]([C:4]1[C:12]([NH2:13])=[CH:11][C:7]2[CH2:8][CH2:9][O:10][C:6]=2[CH:5]=1)([O-])=[O:2].[N:14]#[C:15][NH2:16].[CH]Cl.[OH-].[Na+]>O>[N+:1]1([O-:2])[C:4]2[CH:5]=[C:6]3[O:10][CH2:9][CH2:8][C:7]3=[CH:11][C:12]=2[N:13]=[C:15]([NH2:16])[N:14]=1
参加物反応条件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 9864CyanamideHCID 14798Sodium HydroxideHCID 6432229CID 6432229HCID 130691876-Nitro-2,3-dihydrobenzofuran-5-amine

生成物 1

HCID 25140759HCID 25140759、化合物収率 23%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

A mixture of nitroaniline 194 (7.27 g, 40.4 mmol) and cyanamide (6.79 g, 162 mmol) were mixed together at 100° C., cooled to 50° C., cHCl (15 mL) added carefully and the mixture heated at 100° C. for 4 h. The mixture was cooled to 50° C., 7.5 M NaOH solution added until the mixture was strongly basic and the mixture stirred at 100° C. for 3 h. The mixture was cooled, diluted with water (200 mL), filtered, washed with water (3×50 mL) and dried. The aqueous fraction was extracted with CHCl3 (3×50 mL), dried and the solvent evaporated. The combined solids were purified by chromatography, eluting with a gradient (0-10%) of MeOH/DCM, to give crude amine 195 (1.87 g, 23%) as a yellow powder: mp (MeOH/DCM) 241-246° C. Anal. calcd for C9H8N4O2: C, 52.9; H, 4.0; N, 27.4. Found: C, 53.3; H, 3.8; N, 26.4%.

後処理

  1. additionwere mixed together at 100° C.
  2. temperaturethe mixture heated at 100° C. for 4 h
  3. temperatureThe mixture was cooled to 50° C.
  4. temperatureThe mixture was cooled
  5. filtrationfiltered
  6. washwashed with water (3×50 mL)
  7. customdried
  8. extractionThe aqueous fraction was extracted with CHCl3 (3×50 mL)
  9. customdried
  10. customthe solvent evaporated
  11. customThe combined solids were purified by chromatography
  12. washeluting with a gradient (0-10%) of MeOH/DCM

出典と根拠

ORDレコード
ord-28602d210b8b40068e102483432f1e5e
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989451B2

反応ノート

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