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Cyclopentylamine → Cyclopentylurea

HRID 16232
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인쇄 미리보기

반응식

HRID 16232 반응식
C(Cl)Cl.[CH:4]1([NH2:9])[CH2:8][CH2:7][CH2:6][CH2:5]1.C[Si]([N:14]=[C:15]=[O:16])(C)C>CO>[CH:4]1([NH:9][C:15]([NH2:14])=[O:16])[CH2:8][CH2:7][CH2:6][CH2:5]1
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참가 물질

5

반응물 3

HCID 2906CyclopentylamineHCID 6344DichloromethaneHCID 70696Trimethylsilyl isocyanate

생성물 1

HCID 294526Cyclopentylurea

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a CH2Cl2 solution of cyclopentylamine was added trimethylsilyl isocyanate. The reaction mixture was stirred overnight. To this was added 200 ml of CH3OH, and the mixture was stirred for another 2 hrs. The reaction mixture was concentrated and was titrated using diethyl ether to give an off-white precipitate. The precipitate was filtered through a Buchner funnel to give cyclopentyl urea Compound 30a as a white crystalline solid compound (13.0 g, 86%). To this urea Compound 30a (5.0 g, 38.7 mmol) in acetic acid (11 mL), was added malonic acid (4.0 g, 38.7 mmol) followed by acetic anhydride (18 mL) and the reaction was stirred at 70° C. for 12 hrs. The reaction mixture was concentrated, cooled in an ice bath and titrated using 4/1 EtO2/EtOAc. A pale yellow crystalline solid precipitated out. The precipitate was filtered and washed 2-3 times using cold diethyl ether to obtain a pale yellow solid Compound 30b (2.5 g, 33%).

후처리

  1. stirringthe mixture was stirred for another 2 hrs
  2. concentrationThe reaction mixture was concentrated
  3. customto give an off-white precipitate
  4. filtrationThe precipitate was filtered through a Buchner funnel

출처 및 근거

ORD 기록
ord-fb620b1f1b874ecb900ab3ec42a331aa
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07737155B2

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