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Triethylamine → tert-Butyl 4-[(3-bromophenyl)methyl]piperazine-1-carboxylate

HRID 2080311
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반응식

HRID 2080311 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]Br.[C:10]([N:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1)([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11].C(N(CC)CC)C.C(=O)(O)[O-].[Na+]>C(#N)C>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][N:20]2[CH2:19][CH2:18][N:17]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:22][CH2:21]2)[CH:7]=[CH:8][CH:9]=1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 699793-Bromobenzyl bromideHCID 143452tert-Butyl piperazine-1-carboxylateHCID 516892Sodium Bicarbonate

생성물 1

HCID 53439212tert-Butyl 4-[(3-bromophenyl)methyl]piperazine-1-carboxylate수율 89.7%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

A solution of 3-bromobenzyl bromide (6 g) and Boc-piperazine (4.06 g) in acetonitrile (30 mL) was treated with triethylamine (3.36 mL). The resulting mixture was heated at reflux for 16 hours. After cooling to room temperature, the reaction mixture was treated with saturated sodium bicarbonate solution (20 mL), and then extracted with ethyl acetate (2×30 mL). The organic phases were combined, dried (MgSO4) and concentrated under vacuum. The residue was purified by chromatography on silica (100 g) eluting with ethyl acetate/cyclohexane to give the title compound (6.95 g). LC/MS: m/z, 355, 357 (M+H), 2.40 min.

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux for 16 hours
  3. extractionextracted with ethyl acetate (2×30 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated under vacuum
  6. customThe residue was purified by chromatography on silica (100 g)
  7. washeluting with ethyl acetate/cyclohexane

출처 및 근거

ORD 기록
ord-fca5d91c9e904a32ac6bd6a954f349c8
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932247B2

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