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Sodium Cyanide → HCID 178511085, 화합물

HRID 711934
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HRID 711934 반응식
CS(O[CH2:6][C@H:7]1[CH2:12][CH2:11][C@H:10]([NH:13][C:14]2[C:19]([N+:20]([O-:22])=[O:21])=[CH:18][N:17]=[C:16]3[CH:23]=[CH:24][S:25][C:15]=23)[CH2:9][CH2:8]1)(=O)=O.[C-:26]#[N:27].[Na+]>CS(C)=O.CCOC(C)=O>[N+:20]([C:19]1[C:14]([NH:13][C@H:10]2[CH2:11][CH2:12][C@H:7]([CH2:6][C:26]#[N:27])[CH2:8][CH2:9]2)=[C:15]2[S:25][CH:24]=[CH:23][C:16]2=[N:17][CH:18]=1)([O-:22])=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8929Sodium CyanideHCID 178505298HCID 178505298, 화합물

생성물 1

HCID 178511085HCID 178511085, 화합물

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 8857Ethyl Acetate용매

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온도
90 °C

실험 절차

A mixture of {trans-4-[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}methyl methanesulfonate (0.20 g, 0.52 mmol) and sodium cyanide (0.057 g, 1.2 mmol) in dimethyl sulfoxide (2 mL) was stirred at 90° C. for 4 h. After diluting with EtOAc, the resulting mixture was washed with sat. NaHCO3 solution, water and brine, then concentrated. The residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane) to give the desired product. LCMS calculated for C15H17N4O2S (M+H)+: m/z=317.1. Found: 317.0.

후처리

  1. washthe resulting mixture was washed with sat. NaHCO3 solution, water and brine
  2. concentrationconcentrated
  3. customThe residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane)

출처 및 근거

ORD 기록
ord-f81e97e8643244b3a248f675651a72a6
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181271B2

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