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Imidazole → HCID 68998776, 화합물

HRID 749989
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HRID 749989 반응식
Cl.[NH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[CH2:8][OH:9].N1C=CN=C1.C(N(CC)CC)C.[S:22](Cl)(Cl)=[O:23]>ClCCl>[S@@:22]1(=[O:23])[N:2]2[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]2[CH2:8][O:9]1
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참가 물질

6

반응물 4

HCID 795ImidazoleHCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 69004848(s)-Piperidin-2-ylmethanol hydrochloride

생성물 1

HCID 68998776HCID 68998776, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
2.5 °C

실험 절차

To a solution of (S)-1-Piperidin-2-yl-methanol hydrochloride (3.43 g, 22.63 mmol), imidazole (6.1 g, 88.72 mmol) and triethylamine (7.33 g, 72.42 mmol) in anhydrous dichloromethane (120 mL) at 0-5° C. was added a solution of thionyl chloride (3.2 g, 25.86 mmol) in anhydrous dichloromethane (10 mL) over a period of 45 min. The reaction mixture was stirred at 0-5° C. for 45 min, partitioned with H2O and the aqueous layer was extracted with dichloromethane (2×150 mL). The combined organic layer was washed with H2O, dried over Na2SO4, and concentrated in vacuo to give an orange liquid. Flash column chromatography purification (silica gel, 2% EtOAc in dichloromethane) afforded the title product as a clear, colorless liquid (1.31 g, 36%).

후처리

  1. custompartitioned with H2O
  2. extractionthe aqueous layer was extracted with dichloromethane (2×150 mL)
  3. washThe combined organic layer was washed with H2O
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customto give an orange liquid
  7. customFlash column chromatography purification (silica gel, 2% EtOAc in dichloromethane)

출처 및 근거

ORD 기록
ord-1f366e205ef541f5a2eace37186ff375
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07402684B2

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