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Benzo(d)thiazol-2-amine → 1-(1,3-Benzothiazol-2-yl)-3-[2-(cyclohexen-1-yl)ethyl]thiourea

HRID 233680
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HRID 233680 반응식
[C:1]1([CH2:7][CH2:8][N:9]=[C:10]=[S:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.[NH2:12][C:13]1[S:14][C:15]2[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=2[N:17]=1.C(OCC)(=O)C>CN(C)C=O>[C:1]1([CH2:7][CH2:8][NH:9][C:10]([NH:12][C:13]2[S:14][C:15]3[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=3[N:17]=2)=[S:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1
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참가 물질

5

반응물 3

HCID 8706Benzo(d)thiazol-2-amineHCID 8857Ethyl AcetateHCID 27358811-(2-Isothiocyanatoethyl)cyclohex-1-ene

생성물 1

HCID 30055431-(1,3-Benzothiazol-2-yl)-3-[2-(cyclohexen-1-yl)ethyl]thiourea수율 40.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 2-(1-cyclohexenyl)ethyl isothiocyanate (3.3 g, 20 mmol) and 2-aminobenzothiazole (3.0 g, 20 mmol) in N,N-dimethylformamide (50 mL) was heated at 100° C. for 17.5 h. The reaction was cooled to room temperature, poured into ethyl acetate, washed with water, 1N aqueous HCl, water, saturated sodium bicarbonate, and brine. The organic layer was concentrated and the residue recrystallized from ethyl acetate to provide 2.57 g (40%) of the title product:

후처리

  1. washwashed with water, 1N aqueous HCl, water, saturated sodium bicarbonate, and brine
  2. concentrationThe organic layer was concentrated
  3. customthe residue recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-e7fb97ef7fde4c88babbf60830d864c5
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05593993

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