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1,1'-Thiocarbonyldi-2(1H)-pyridone → 3-Isothiocyanato-6-methylisoquinoline

HRID 250130
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HRID 250130 반응식
[C:1](N1C=CC=CC1=O)(N1C=CC=CC1=O)=[S:2].[CH3:17][C:18]1[CH:19]=[C:20]2[C:25](=[CH:26][CH:27]=1)[CH:24]=[N:23][C:22]([NH2:28])=[CH:21]2>ClCCl>[N:28]([C:22]1[N:23]=[CH:24][C:25]2[C:20]([CH:21]=1)=[CH:19][C:18]([CH3:17])=[CH:27][CH:26]=2)=[C:1]=[S:2]
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참가 물질

4

반응물 2

HCID 8531621,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 187279006-Methylisoquinolin-3-amine

생성물 1

HCID 574766053-Isothiocyanato-6-methylisoquinoline수율 47.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
40 °C

실험 절차

To a solution of 1,1′-thiocarbonyldipyridin-2(1H)-one (220 mg, 0.948 mmol) in dichloromethane (10 mL) at ambient temperature was added 6-methylisoquinolin-3-amine (125 mg, 0.790 mmol). The reaction mixture was placed into a preheated oil-bath and stirred at 40° C. for 18 h, then removed from the oil-bath and cooled to ambient temperature. The mixture was concentrated and the crude material was purified by silica gel chromatography (5-30% ethyl acetate in hexanes) to afford 3-isothiocyanato-6-methylisoquinoline (75 mg, 0.375 mmol, 47.4% yield), as an off-white solid. 1H NMR (400 MHz, CDCl3) δ ppm 9.03 (s, 1H), 7.88 (d, J=8.24 Hz, 1H), 7.56 (s, 1H), 7.46 (dd, J=8.24, 1.53 Hz, 1H), 7.39 (s, 1H) 2.57 (s, 3H). MS (LC/MS) R.T.=1.92; [M+H]+=201.13.

후처리

  1. customThe reaction mixture was placed into a preheated oil-bath
  2. customremoved from the oil-bath
  3. temperaturecooled to ambient temperature
  4. concentrationThe mixture was concentrated
  5. customthe crude material was purified by silica gel chromatography (5-30% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-1a945c0cb3c643b1a0b37047bf6304d5
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863291B2

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