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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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creatinine → HCID 136174789, 화합물

HRID 904171
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HRID 904171 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 588creatinineHCID 11286446Furan, 2-isocyanato-

생성물 1

HCID 136174789HCID 136174789, 화합물수율 8.3%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6228Dimethylformamide용매

실험 절차

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.)

후처리

  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

출처 및 근거

ORD 기록
ord-7f1293c511394cd2a6fef3ae92bebe96
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04230713

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