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Hydrochloric Acid → HCID 178485080、化合物

HRID 261416
ノート
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反応式

HRID 261416 の反応式
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:19][CH3:20])=[N:16][C:17]#[N:18])[N:9]=1)[C:2]([NH2:4])=[NH:3].[ClH:21].C[OH:23]>>[ClH:21].[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:19][CH3:20])=[N:16][C:17](=[O:23])[NH2:18])[N:9]=1)[C:2]([NH2:4])=[NH:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 313Hydrochloric Acid2 回HCID 887MethanolHCID 178485064HCID 178485064、化合物

生成物 1

HCID 178485080HCID 178485080、化合物

実験手順

A mixture of 2-guanidino-4-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]thiazole (1.0 g.), and 2.5 N hydrochloric acid (12 ml.) was heated for four minutes on the steam bath. On cooling a white solid precipitated which was applied to Merck 60 F-254 preparative thin layer chromatography plates and eluted with chloroform/methanol/ammonia (s.g. 0.880) 7:3:0.5 v/v/v. The yellow foam obtained was dissolved in methanol and methanolic hydrogen chloride added. The solution was evaporated to dryness and the residue crystallized from methanol to give 2-guanidino-4-[2-(2-carbamoyl-3-methylguanidino)ethylthiomethyl]thiazole hydrochloride, m.p. 148°-150° C.

後処理

  • temperaturewas heated for four minutes on the steam bath
  • temperatureOn cooling a white solid
  • customprecipitated which
  • washeluted with chloroform/methanol/ammonia (s.g. 0.880) 7:3:0.5 v/v/v
  • customThe yellow foam obtained
  • customThe solution was evaporated to dryness
  • customthe residue crystallized from methanol
  • 出典と根拠

    ORDレコード
    ord-6f2a8c30e7bd4f5abcd8b7b5f2a3ec4a
    出典データセット
    uspto-grants-1979_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04165378

    反応ノート

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