1,2-Dichloroethane → (S)-tert-butyl 3-((R)-2-hydroxy-2-phenylethylcarbamoyl)hex-5-enoate

HRID 41070

반응식

HRID 41070 반응식
[C:1]([O:5][C:6](=[O:15])[CH2:7][C@H:8]([CH2:12][CH:13]=[CH2:14])[C:9]([OH:11])=O)([CH3:4])([CH3:3])[CH3:2].C(Cl)CCl.C1C=CC2N(O)N=[N:26]C=2C=1.N[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[C@H:37]([OH:39])[CH3:38].CCN(C(C)C)C(C)C>CN(C=O)C.CN(C1C=CN=CC=1)C>[OH:39][C@H:37]([C:32]1[CH:33]=[CH:34][CH:35]=[CH:36][CH:31]=1)[CH2:38][NH:26][C:9]([C@@H:8]([CH2:12][CH:13]=[CH2:14])[CH2:7][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:15])=[O:11]

참가 물질

8

반응물 5

HCID 111,2-DichloroethaneHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 10920569(R)-2-amino-phenylethanolHCID 16053367(S)-2-[2-(tert-Butoxy)-2-oxoethyl]pent-4-enoic Acid

생성물 1

HCID 67312340(S)-tert-butyl 3-((R)-2-hydroxy-2-phenylethylcarbamoyl)hex-5-enoate수율 85%

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6228Dimethylformamide용매

실험 절차

To a solution of (S)-2-(2-tert-butoxy-2-oxoethyl)pent-4-enoic acid (0.947 g, 4.42 mmol) (described by Stanton, B. Z. et al. Nat. Chem. Biol. 2009, 5, 154-156) in DMF (31.6 mL) cooled in an ice/water bath was added EDC (1.27 g, 6.63 mmol) and HOBt (0.896 g, 6.63 mmol) and the resulting solution was stirred 30 min. (R)-2-amino-phenylethanol (0.667 g, 4.86 mmol), iPr2NEt (2.31 mL, 13.3 mmol) and DMAP (0.108 g, 0.884 mmol) were subsequently added and the reaction mixture was slowly warmed to rt and stirred for 16 h at which point LC-MS analysis indicated complete consumption of starting material. The reaction mixture was diluted with saturated NH4Cl and EtOAc and the layers separated. The aqueous was extracted 2× with EtOAc and the combined organic extracts were washed with 1 N HCl and brine, dried over Na2SO4, filtered, and concentrated. The crude product was purified using silica gel chromatography (MeOH/CH2Cl2 gradient) to yield 1.25 g of desired product as a light yellow oil in 85% yield. LRMS (M+Na)+: 356.2.

후처리

  1. additionwere subsequently added
  2. customconsumption of starting material
  3. additionThe reaction mixture was diluted with saturated NH4Cl and EtOAc
  4. customthe layers separated
  5. extractionThe aqueous was extracted 2× with EtOAc
  6. washthe combined organic extracts were washed with 1 N HCl and brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified

출처 및 근거

ORD 기록
ord-fba568ae791d4759969f39512fca942b
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08530456B2

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