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Methanesulfonic Acid → 1-(cyclopropylmethyl)-5-methoxy-1H-benzotriazole

HRID 1626979
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HRID 1626979 반응식
[CH:1]1([CH2:4][NH:5][C:6]2[C:7]([NH2:14])=[CH:8][C:9]([O:12][CH3:13])=[CH:10][CH:11]=2)[CH2:3][CH2:2]1.CS(O)(=O)=O.[N:20](OCCC(C)C)=O>C(O)C.C(OCC)(=O)C>[CH:1]1([CH2:4][N:5]2[C:6]3[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][C:7]=3[N:14]=[N:20]2)[CH2:2][CH2:3]1
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참가 물질

6

반응물 3

HCID 6395Methanesulfonic AcidHCID 8053Isoamyl NitriteHCID 70197765HCID 70197765, 화합물

생성물 1

HCID 686570341-(cyclopropylmethyl)-5-methoxy-1H-benzotriazole

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8857Ethyl Acetate용매

실험 절차

N1-(Cyclopropylmethyl)-4-methoxybenzene-1,2-diamine (10.8 g, 56.2 mmol) was dissolved in ethanol (80 mL) and treated with methanesulfonic acid (3.65 ml, 56.2 mmol) followed by isoamyl nitrite (7.56 ml, 56.2 mmol). The mixture was stirred for 15 minutes, diluted with ethyl acetate (1500 mL) and washed with aqueous saturated bicarbonate solution (500 mL×2). The organic extracts were concentrated in vacuo and the residue was purified by silica gel gradient chromatography (5-50% ethyl acetate in heptanes), providing the titled compound as a tan solid.

후처리

  1. washwashed with aqueous saturated bicarbonate solution (500 mL×2)
  2. concentrationThe organic extracts were concentrated in vacuo
  3. customthe residue was purified by silica gel gradient chromatography (5-50% ethyl acetate in heptanes)

출처 및 근거

ORD 기록
ord-7fe7d1b44e104bf485cb46bdaa65681d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785482B2

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