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1-Pyrrolidineethanamine → Tert-butyl 4-[[2-(1-pyrrolidinyl)ethyl]amino]benzoate

HRID 131280
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인쇄 미리보기

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HRID 131280 반응식
F[C:2]1[CH:14]=[CH:13][C:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])=[CH:4][CH:3]=1.[NH2:15][CH2:16][CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1>O>[N:18]1([CH2:17][CH2:16][NH:15][C:2]2[CH:14]=[CH:13][C:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])=[CH:4][CH:3]=2)[CH2:22][CH2:21][CH2:20][CH2:19]1
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참가 물질

4

반응물 2

HCID 13441-PyrrolidineethanamineHCID 2736444Tert-butyl 4-fluorobenzoate

생성물 1

HCID 69299992Tert-butyl 4-[[2-(1-pyrrolidinyl)ethyl]amino]benzoate수율 51%

시약·촉매·용매 1

HCID 962Water용매

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온도
120 °C

실험 절차

A mixture of tert-butyl 4-fluorobenzoate (2.14 g) and 1-(2-aminoethyl)pyrrolidine (1 mL) is stirred at 120° C. for one day. After cooling, to the reaction mixture is added water and the mixture is extracted with ethyl acetate (×2). The extract is concentrated by centrifugal concentrator and the residue is purified by flash column chromatography on NH-silica gel (Solvent; n-hexane:ethyl acetate=8:1→4:1) to give tert-butyl 4-[[2-(1-pyrrolidinyl)ethyl]amino]benzoate (1.62 g, yield; 51%) as an oil. MS (APCI) m/z: 291 [M+H]+

후처리

  1. temperatureAfter cooling, to the reaction mixture
  2. extractionthe mixture is extracted with ethyl acetate (×2)
  3. concentrationThe extract is concentrated by centrifugal concentrator
  4. customthe residue is purified by flash column chromatography on NH-silica gel (Solvent; n-hexane:ethyl acetate=8:1→4:1)

출처 및 근거

ORD 기록
ord-e02528d578e044078b957fe836e2bf39
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07384952B2

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