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creatinine → HCID 136174789、化合物

HRID 904171
ノート
印刷プレビュー

反応式

HRID 904171 の反応式
[CH3:1][N:2]1[C:7]([NH2:8])=[N:6][C:4](=[O:5])[CH2:3]1.[O:9]1[CH:13]=[CH:12][CH:11]=[C:10]1[N:14]=[C:15]=[O:16]>CN(C=O)C.C1(C)C=CC=CC=1>[O:9]1[CH:13]=[CH:12][CH:11]=[C:10]1[NH:14][C:15]([N:8]=[C:7]1[NH:6][C:4](=[O:5])[CH2:3][N:2]1[CH3:1])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 588creatinineHCID 11286446Furan, 2-isocyanato-

生成物 1

HCID 136174789HCID 136174789、化合物収率 8.3%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 6228Dimethylformamide溶媒

実験手順

To a stirred mixture of 6.9 g (60 mM) of creatinine in 100 ml of anhydrous DMF was added a solution of 6.5 g (60 mM) of 2-furanyl isocyanate in 75 ml of toluene. After stirring the mixture 1 hr. at 25° C. and then 1 hr. at 55° C., the solvents were removed in vacuo and the residue taken up in ethyl acetate and washed with water. The solvent was removed and the residue chromatographed over silica gel using ether-ethyl acetate (4:1) as the eluant. The fractions containing the product were combined and concentrated to leave 1.1 g of the above urea as an off-white solid, m.p. 173°-175° C. (dec.)

後処理

  1. customat 25° C.
  2. custom1 hr
  3. customat 55° C., the solvents were removed in vacuo
  4. washwashed with water
  5. customThe solvent was removed
  6. customthe residue chromatographed over silica gel
  7. additionThe fractions containing the product
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7f1293c511394cd2a6fef3ae92bebe96
出典データセット
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04230713

反応ノート

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