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1,4-Dioxane hydrochloride → HCID 89924032, 화합물

HRID 2200371
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HRID 2200371 반응식
[C:1]([C:3]1[CH2:7][CH2:6][C@@H:5]([N:8]2[CH2:13][CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10][CH2:9]2)[CH:4]=1)#[N:2].O1CCOCC1.Cl>ClCCl>[N:8]1([C@@H:5]2[CH2:6][CH2:7][C:3]([C:1]#[N:2])=[CH:4]2)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1
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참가 물질

4

반응물 2

HCID 204431481,4-Dioxane hydrochlorideHCID 89938204HCID 89938204, 화합물

생성물 1

HCID 89924032HCID 89924032, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
25 °C

실험 절차

To a solution of (R)-tert-butyl 4-(3-cyanocyclopent-2-en-1-yl)piperazine-1-carboxylate (13 g, 46.9 mmol) in dry dichloromethane (30 ml) was added slowly hydrochloric acid 1,4 dioxane (100 ml, 4M solution) in a drop wise manner 0° C. The reaction mixture was stirred at 25° C. for 3 h. The progress of the reaction was monitored by TLC. The reaction mixture was then concentrated under reduced pressure. The residue was diluted with dichloromethane (100 ml) and treated with methanolic ammonia (50 ml, 7M solution) and stirred for 30 minutes. The reaction mixture was then evaporated under reduced pressure to obtain crude product which was purified by flash column chromatography over silica gel (100-200 mesh) using 10% methanol in dichloromethane as an eluent to obtain title compound ((7 g, 84%).

후처리

  1. concentrationThe reaction mixture was then concentrated under reduced pressure
  2. additionThe residue was diluted with dichloromethane (100 ml)
  3. additiontreated with methanolic ammonia (50 ml, 7M solution)
  4. stirringstirred for 30 minutes
  5. customThe reaction mixture was then evaporated under reduced pressure
  6. customto obtain crude product which
  7. customwas purified by flash column chromatography over silica gel (100-200 mesh)

출처 및 근거

ORD 기록
ord-5bc63acd48cf4379a53d16f0dc67ce1e
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09359367B2

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