2-Bromo-4-chloroaniline → 2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzene

HRID 1247054

반응식

HRID 1247054 반응식
Cl[C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.[Br:13][C:14]1[CH:20]=[C:19]([Cl:21])[CH:18]=[CH:17][C:15]=1[NH2:16].C(N(CC)C(C)C)(C)C.[C:31]([N:38]1[CH2:43][CH2:42][NH:41][CH2:40][CH2:39]1)([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32]>ClCCl>[C:31]([N:38]1[CH2:39][CH2:40][N:41]([C:2]([NH:16][C:15]2[CH:17]=[CH:18][C:19]([Cl:21])=[CH:20][C:14]=2[Br:13])=[O:4])[CH2:42][CH2:43]1)([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32]

참가 물질

6

반응물 4

HCID 701102-Bromo-4-chloroanilineHCID 81531DiisopropylethylamineHCID 94429TriphosgeneHCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 219065382-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzene수율 191.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a stirring solution of triphosgene (2.7 g, 9.0 mmol) in dichloromethane (100 mL) was added, dropwise via an addition funnel, a solution of 2-bromo-4-chloroaniline (5 g, 24.2 mmol) and N,N-diisopropylethylamine (6.9 g, 53.2 mmol) in dichloromethane (50 mL). After complete addition and an additional hour, a solution of N-Boc-piperazine (5 g, 26.6 mmol) in dichloromethane (50 mL) was added. After stirring overnight, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed consecutively with 1 M citric acid, brine, sat. aq sodium bicarbonate and finally with brine, then dried with MgSO4, filtered and concentrated in vacuo. The residue was then dissolved in a minimal amount of chloroform and chromatographed over silica gel, eluting with 20% ethyl acetate in hexanes followed by 30% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo and the resulting solid was suspended in diethyl ether, sonicated and then filtered and dried in vacuo to give 7.2 g (71%) of a white powder.

후처리

  1. additionAfter complete addition
  2. customthe solvent was removed in vacuo
  3. customthe residue was partitioned between ethyl acetate and water
  4. customThe organic phase was separated
  5. washwashed consecutively with 1 M citric acid, brine, sat. aq sodium bicarbonate and finally with brine
  6. dry with materialdried with MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. dissolutionThe residue was then dissolved in a minimal amount of chloroform
  10. customchromatographed over silica gel
  11. washeluting with 20% ethyl acetate in hexanes
  12. additionThe product containing fractions
  13. concentrationconcentrated in vacuo
  14. customsonicated
  15. filtrationfiltered
  16. customdried in vacuo

출처 및 근거

ORD 기록
ord-02c2ef16fc854b0c837365bddf876291
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07129245B2

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