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Hydrochloric Acid → 1-Cyclopropyl-2-(5-methyl-1,3,4-oxadiazol-2-yl)propan-2-amine

HRID 1480243
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HRID 1480243 반응식
[CH:1]1([CH2:4][C:5]([NH:13]S(C(C)(C)C)=O)([CH3:12])[C:6]2[O:7][C:8]([CH3:11])=[N:9][N:10]=2)[CH2:3][CH2:2]1.Cl.O1CCOCC1>CO>[CH:1]1([CH2:4][C:5]([C:6]2[O:7][C:8]([CH3:11])=[N:9][N:10]=2)([NH2:13])[CH3:12])[CH2:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 90203435HCID 90203435, 화합물

생성물 1

HCID 902046221-Cyclopropyl-2-(5-methyl-1,3,4-oxadiazol-2-yl)propan-2-amine수율 50%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of N-[2-cyclopropyl-1-methyl-1-(5-methyl-1,3,4-oxadiazol-2-yl)ethyl]-2-methyl-propane-2-sulfinamide (example 173a, 520 mg, 1.46 mmol) in MeOH (8 ml) was added a 4M solution of hydrochloric acid in dioxane (729 μl, 2.92 mmol). The reaction mixture was stirred at room temperature for 1 hour. Reaction was quenched by addition of potassium carbonate and stirred for 15 minutes. The insolubles were removed by filtration and the filtrate was evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a dichloromethane-methanol gradient to yield the title compound (130 mg, 50%). MS (ESI, m/z): 182.2 (M+H+).

후처리

  1. customReaction
  2. customwas quenched by addition of potassium carbonate
  3. stirringstirred for 15 minutes
  4. customThe insolubles were removed by filtration
  5. customthe filtrate was evaporated down to dryness
  6. customThe crude material was purified by flash chromatography on silica eluting with a dichloromethane-methanol gradient

출처 및 근거

ORD 기록
ord-42c909ab5fa149e1a28074b79c90a81c
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409866B2

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