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Aminoacetonitrile hydrochloride → 5-Amino-1-(1,2,3,4-tetrahydronaphthalen-2-yl)-1,3-dihydroimidazole-2-thione

HRID 863071
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HRID 863071 반응식
[N:1]([CH:4]1[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5]1)=[C:2]=[S:3].Cl.[NH2:15][CH2:16][C:17]#[N:18]>C(N(CC)CC)C>[NH2:15][C:16]1[N:1]([CH:4]2[CH2:13][CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH2:5]2)[C:2](=[S:3])[NH:18][CH:17]=1
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참가 물질

4

반응물 2

HCID 11491918Aminoacetonitrile hydrochlorideHCID 196994682-Isothiocyanato-1,2,3,4-tetrahydronaphthalene

생성물 1

HCID 196994295-Amino-1-(1,2,3,4-tetrahydronaphthalen-2-yl)-1,3-dihydroimidazole-2-thione

시약·촉매·용매 1

HCID 8471Triethylamine용매

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온도
60 °C

실험 절차

A mixture of 2-isothiocyano-1,2,3,4-tetrahydronaphthalene (1.92 g, 10.1 mol), prepared as in Example 10, and aminoacetonitrile hydrochloride (0.94 g, 10.1 mmol) in 1.41 mL of triethylamine was heated at 60° C. for 1 hour. The solvent was evaporated and the residue was purified by flash chromatography (elution: methylene chloride followed by 3% methanol in methylene chloride). The purified residue was recrystallized from ethyl acetate/hexane. The residue (1.06 g) and 44 mL of 0.1N potassium hydroxide was stirred under nitrogen for 15 minutes. The residue was isolated by filtration, washed with water, air dried and then stirred with methylene chloride. Filtration and drying gave 5-amino-1-(1,2,3,4-tetrahydronaphthalen-2-yl)-1,3-dihydroimidazole-2-thione, m.p. 169°-171° C.

후처리

  1. customThe solvent was evaporated
  2. customthe residue was purified by flash chromatography (elution: methylene chloride followed by 3% methanol in methylene chloride)
  3. customThe purified residue was recrystallized from ethyl acetate/hexane
  4. customThe residue was isolated by filtration
  5. washwashed with water, air
  6. customdried
  7. stirringstirred with methylene chloride
  8. filtrationFiltration
  9. customdrying

출처 및 근거

ORD 기록
ord-723a0aba5c824f788469e0c9d093be21
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05719280

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