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Triethylamine → Methyl 4-[2-[4-(4-pyrimidinyl)piperazin-1-yl]acetyl]phenoxyacetate

HRID 864788
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HRID 864788 반응식
[N:1]1([C:7]2[CH:12]=[CH:11][N:10]=[CH:9][N:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.C(N(CC)CC)C.Br[CH2:21][C:22]([C:24]1[CH:35]=[CH:34][C:27]([O:28][CH2:29][C:30]([O:32][CH3:33])=[O:31])=[CH:26][CH:25]=1)=[O:23]>C(#N)C>[N:10]1[CH:11]=[CH:12][C:7]([N:1]2[CH2:6][CH2:5][N:4]([CH2:21][C:22]([C:24]3[CH:35]=[CH:34][C:27]([O:28][CH2:29][C:30]([O:32][CH3:33])=[O:31])=[CH:26][CH:25]=3)=[O:23])[CH2:3][CH2:2]2)=[N:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 243438Methyl 4-bromoacetylphenoxyacetateHCID 183211374-(Piperazin-1-yl)pyrimidine

생성물 1

HCID 18918603Methyl 4-[2-[4-(4-pyrimidinyl)piperazin-1-yl]acetyl]phenoxyacetate수율 26.1%

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

To a mixture of 4-(1-piperazinyl)pyrimidine (preparation described in DE 2316920) (1.57 g) and triethylamine (3.87 g) in acetonitrile (40 ml) at room temperature was added dropwise over about 0.5 hour a solution of methyl 4-bromoacetylphenoxyacetate (2.73 g) in acetonitrile (25 ml). On completion of the addition the reaction mixture was stirred at room temperature for 2 days. The precipitated solid was filtered off, washed with acetonitrile and the combined filtrate and washings evaporated to dryness. The resultant red oil was purified by flash chromatography, first on silica by elution with 1-5% v/v methanol/dichloromethane, then on neutral alumina by elution with 3% v/v methanol/dichloromethane, to yield the title compound (0.92 g) as an off-white solid: NMR (CDCl3) δ2.69 (4H, m), 3.72 (4H, m), 3.80 (2H, s), 3.82 (3H, s), 4.71 (2H, s), 6.49 (1H, m), 6.94 (2H, d), 8.01 (2H, d), 8.20 (1H, d), 8.60 (1H, s); m/Z 371 (M+H)+ ; calculated for C19H22N4O4. 0.4 H2O: C 60.4%; H, 6.09%; N, 14.8%; found: C, 60.7%; H, 6.2%; N, 14.7%.

후처리

  1. additionOn completion of the addition the reaction mixture
  2. filtrationThe precipitated solid was filtered off
  3. washwashed with acetonitrile
  4. customthe combined filtrate and washings evaporated to dryness
  5. customThe resultant red oil was purified by flash chromatography, first on silica by elution with 1-5% v/v methanol/dichloromethane
  6. washon neutral alumina by elution with 3% v/v methanol/dichloromethane

출처 및 근거

ORD 기록
ord-cdecd2a4a6604fe7835629cb99d3333c
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05563141

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