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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thiourea → 6-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine

HRID 2059050
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HRID 2059050 반응식
[NH2:1][C:2]([NH2:4])=[S:3].Br[CH:6]1[CH2:11][CH:10]([CH3:12])[CH2:9][CH2:8][C:7]1=O>C(O)C>[NH2:1][C:2]1[S:3][C:6]2[CH2:11][CH:10]([CH3:12])[CH2:9][CH2:8][C:7]=2[N:4]=1
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참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 124904552-Bromo-4-methylcyclohexan-1-one

생성물 1

HCID 3469226-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Thiourea (22.3 g., 0.29 mole) was slurried in 275 ml. of ethanol. 2-Bromo-4-methylcyclohexanone was added and the mixture heated to reflux for 75 minutes. The reaction mixture was cooled to room temperature and the crude product recovered as the hydrobromide salt by filtration. The crude salt was dissolved in warm water, filtered and made basic with ammonium hydroxide to precipitate the free base as an oil, which crystallized on cooling. Purified 2-amino-4,5,6,7-tetrahydro-6-methylbenzthiazole (25.2 g., m.p. 98°-100° C.) was obtained by recrystallization from cyclohexane.

후처리

  1. temperaturethe mixture heated
  2. temperatureto reflux for 75 minutes
  3. filtrationthe crude product recovered as the hydrobromide salt by filtration
  4. dissolutionThe crude salt was dissolved in warm water
  5. filtrationfiltered
  6. customto precipitate the free base as an oil, which
  7. customcrystallized
  8. temperatureon cooling

출처 및 근거

ORD 기록
ord-6c21d931920e406a87f2ad2e4e7c0c6d
출처 데이터셋
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04321372

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