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Ammonia → HCID 178433513、化合物

HRID 1075158
ノート
印刷プレビュー

反応式

HRID 1075158 の反応式
N.C(=O)([O-])[O-].[Na+].[Na+].[Cl:8][C:9]1[C:10](=S)[NH:11][C:12](=[O:16])[NH:13][C:14]=1[CH3:15]>O.[Ni]>[CH3:15][C:14]1[C:9]([Cl:8])=[CH:10][NH:11][C:12](=[O:16])[N:13]=1
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 3

HCID 222AmmoniaHCID 10340Sodium CarbonateHCID 20494272HCID 20494272、化合物

生成物 1

HCID 178433513HCID 178433513、化合物収率 53%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 962Water溶媒

実験手順

Conc. aqueous ammonia (200 ml) and sodium carbonate (0.012 mol) were added to Raney-Ni (20 g) in water (200 ml) followed by the addition of 5-chloro-6-methyl-4-thiouracil (0.023 mol). The reaction mixture was stirred at room temperature for 1 hr and then heated under reflux for 3 hr. The catalyst was removed from the cold reaction mixture and the filtrate evaporated. The residual material was stirred in 5 N NaOH (20 ml) and the sodium salt filtered off from the ice-cold mixture and washed with abs. ethanol and acetone. The product was recrystallised from aqueous ethanol; yield 53%, m.p. 300° C. (decomp.); For elemental analysis the sodium salt in aqueous solution was neutralised with HCl. Found: C, 41.40; H, 3.60. Calc. for C5H5ClN2O: C, 41.54; H, 3.48.

後処理

  1. temperatureheated
  2. temperatureunder reflux for 3 hr
  3. customThe catalyst was removed from the cold reaction mixture
  4. customthe filtrate evaporated
  5. stirringThe residual material was stirred in 5 N NaOH (20 ml)
  6. filtrationthe sodium salt filtered off from the ice-cold mixture
  7. washwashed with abs
  8. customThe product was recrystallised from aqueous ethanol

出典と根拠

ORDレコード
ord-a124b5eb7c144d98ac21ec9afbba5503
出典データセット
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04395406

反応ノート

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