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Hydrochloric Acid → N1-(3-dimethylamino-propyl)-4-ethynyl-N1-methyl-benzene-1,2-diamine

HRID 446241
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HRID 446241 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH3:16])[CH2:10][CH2:11][CH2:12][N:13]([CH3:15])[CH3:14])=[C:5]([N+:17]([O-])=O)[CH:4]=1)#[CH:2].CCO.Cl>[Fe].C1COCC1>[CH3:15][N:13]([CH3:14])[CH2:12][CH2:11][CH2:10][N:9]([CH3:16])[C:6]1[C:5]([NH2:17])=[CH:4][C:3]([C:1]#[CH:2])=[CH:8][CH:7]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 86602587N-(4-ethynyl-2-nitro-phenyl)-N,N',N'-trimethyl-propane-1,3-diamine

생성물 1

HCID 59427940N1-(3-dimethylamino-propyl)-4-ethynyl-N1-methyl-benzene-1,2-diamine

시약·촉매·용매 2

HCID 23925Iron촉매HCID 8028Tetrahydrofuran
용매

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온도
90 °C

실험 절차

To N-(4-ethynyl-2-nitro-phenyl)-N,N′,N′-trimethyl-propane-1,3-diamine (730 mg, 2.79 mmol), EtOH (40 mL) and THF (13 mL) was added concentrated HCl (1.0 mL) and iron metal (10.6 g, 191 mmol). A reflux condenser was attached and the mixture was heated overnight at 90° C. The cooled mixture was filtered through a pad of Celite, concentrated and purified by flash chromatography (90:10:1 CH2Cl2/MeOH/NH4OH) to yield N1-(3-dimethylamino-propyl)-4-ethynyl-N1-methyl-benzene-1,2-diamine. MS m/z=232 [M+1]+. Calc'd for C14H21N3: 231.34.

후처리

  1. customA reflux condenser was attached
  2. filtrationThe cooled mixture was filtered through a pad of Celite
  3. concentrationconcentrated
  4. custompurified by flash chromatography (90:10:1 CH2Cl2/MeOH/NH4OH)

출처 및 근거

ORD 기록
ord-0b42f8369084459991ba6ff164dae0ff
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476434B2

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