2-Bromoethanol → cis(+/-)4-Azido-1-(2-hydroxyethyl)piperidin-3-ol

HRID 255202노트

반응식

HRID 255202 반응식
[N:1]([C@H:4]1[CH2:9][CH2:8][NH:7][CH2:6][C@H:5]1[OH:10])=[N+:2]=[N-:3].C(N(CC)C(C)C)(C)C.Br[CH2:21][CH2:22][OH:23].C(OC(N[C@@H]1CCN(CCO)C[C@@H]1C(OC)=O)=O)C1C=CC=CC=1>>[N:1]([C@H:4]1[CH2:9][CH2:8][N:7]([CH2:21][CH2:22][OH:23])[CH2:6][C@H:5]1[OH:10])=[N+:2]=[N-:3]

참가 물질

5

반응물 4

HCID 108982-BromoethanolHCID 81531DiisopropylethylamineHCID 58745547Cis(+/-)4-azidopiperidin-3-olHCID 66774341Methyl(3S,4R)-4-{[(benzyloxy)carbonyl]amino}-1-(2-hydroxyethyl)piperidine-3-carboxylate

생성물 1

HCID 86642610cis(+/-)4-Azido-1-(2-hydroxyethyl)piperidin-3-ol수율 93%

실험 절차

Cis(±)4-azidopiperidin-3-ol (prepared following the procedure described in WO 2005/066176 for the chiral material) (0.945 g, 6.65 mmol), N,N-diisopropylethylamine (1.7 mL, 10 mmol) and 2-bromoethanol (0.61 mL, 8.64 mmol) were reacted as described for Intermediate 37, except heating for one hour. The solvent was removed under reduced pressure. The residue was taken up in dichloromethane (100 mL), washed with 1M sodium hydroxide solution (30 mL) and the aqueous phase was back extracted five times with dichloromethane (5×100 mL). The combined organic phases were dried over sodium sulfate. Chromatography on silica gel with dichloromethane/methanol 3:1 gave 1.15 g (93%) of the product as a colorless oil.

후처리

  1. customwere reacted
  2. temperatureexcept heating for one hour
  3. customThe solvent was removed under reduced pressure
  4. washwashed with 1M sodium hydroxide solution (30 mL)
  5. extractionthe aqueous phase was back extracted five times with dichloromethane (5×100 mL)
  6. dry with materialThe combined organic phases were dried over sodium sulfate

출처 및 근거

ORD 기록
ord-3b2d1dd513a54ba4bc96d518b3adddce
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07875715B2

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