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Hydroxyamine hydrochloride → HCID 178453351, 화합물

HRID 632435
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HRID 632435 반응식
C(=O)(O)[O-].[Na+].Cl.[NH2:7][OH:8].[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22]#[N:23])([CH3:21])[CH2:17][CH:18]1[CH2:20][CH2:19]1)([CH3:12])([CH3:11])[CH3:10]>O.C(O)C>[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22](=[NH:23])[NH:7][OH:8])([CH3:21])[CH2:17][CH:18]1[CH2:19][CH2:20]1)([CH3:10])([CH3:12])[CH3:11]
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참가 물질

6

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 71087668(Cyano-cyclopropylmethyl-methyl-methyl)-carbamic acid tert-butyl ester

생성물 1

HCID 178453351HCID 178453351, 화합물수율 66%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water
용매

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온도
80 °C

실험 절차

Sodium bicarbonate (247.52 mg, 2.94 mmol) was dissolved in water (2 mL) and hydroxylamine hydrochloride (204.747 mg, 2.94 mmol) was added. A solution of (1-cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid tert-butyl ester (600 mg, 2.69 mmol) in ethanol (10 mL) was added thereto and the resulting reaction mixture was heated at 80° C. for 12 hours. After evaporation of solvents, the residue was dissolved with ethyl acetate (20 mL) and then filtered. The filtrate was concentrated in vacuo. The residue was purified by chromatography (silica gel, 25 g, 3:7 ethyl acetate/n-hexane) to give the title compound (450 mg, 66%) as white solid; LC-MS (UV peak area, ESI) 100%, 258.4 (M+H).

후처리

  1. customthe resulting reaction mixture
  2. customAfter evaporation of solvents
  3. dissolutionthe residue was dissolved with ethyl acetate (20 mL)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo
  6. customThe residue was purified by chromatography (silica gel, 25 g, 3:7 ethyl acetate/n-hexane)

출처 및 근거

ORD 기록
ord-1f49112466cb4dd5b04f834114ff76ac
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09321727B2

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