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Water → HCID 18752889, 화합물

HRID 1838068
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HRID 1838068 반응식
[NH2:1][C:2]1[C:7](/[CH:8]=[CH:9]/[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:6][C:5]([Cl:17])=[CH:4][N:3]=1.[BH4-].[Na+].O>C(O)C>[NH2:1][C:2]1[C:7]([CH2:8][CH2:9][C:10]([O:12][C:13]([CH3:15])([CH3:14])[CH3:16])=[O:11])=[CH:6][C:5]([Cl:17])=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 86590075HCID 86590075, 화합물

생성물 1

HCID 18752889HCID 18752889, 화합물수율 65%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of t-butyl (E)-3-(2-amino-5-chloro-3-pyridinyl)-2-propenoate (500 mg, 2.0 mmol) in ethanol (10 ml) at RT was added sodium borohydride (317 mg, 8.4 mmol) portionwise and the mixture stirred for 16 h. After the addition of water, the ethanol removed in vacuo and the mixture extracted with diethyl ether. The ethereal extracts were dried over MgSO4, evaporated to dryness and purified by column chromatography upon silica gel using hexane-EtOAc (7:3) as eluant to give t-butyl 3-(2-amino-5-chloro-3-pyridinyl)propanoate as a colourless oil (340 mg, 1.3 mmol).

후처리

  1. customthe ethanol removed in vacuo
  2. extractionthe mixture extracted with diethyl ether
  3. dry with materialThe ethereal extracts were dried over MgSO4
  4. customevaporated to dryness
  5. custompurified by column chromatography upon silica gel

출처 및 근거

ORD 기록
ord-10185af7e1274f4690ae22bc23c3dbfa
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06673789B2

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