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Triethylamine → HCID 178498696, 화합물

HRID 1425688
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HRID 1425688 반응식
O[CH2:2][C@@H:3]([NH:8][C:9]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]([O:6][CH3:7])=[O:5].CS(Cl)(=O)=O.CCN(CC)CC.S([O-])(=O)(=O)C>C(Cl)Cl.COCCOC>[C:9]([N@@:8]1[CH2:2][CH:3]1[C:4]([O:6][CH3:7])=[O:5])([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
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참가 물질

7

반응물 4

HCID 8471Triethylamine2회HCID 31297Methanesulfonyl chlorideHCID 85257MethanesulfonateHCID 7438296Methyl trityl-D-serinate

생성물 1

HCID 178498696HCID 178498696, 화합물수율 74%

시약·촉매·용매 2

HCID 6344Dichloromethane
용매
HCID 80711,2-Dimethoxyethane용매

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온도
0 °C

실험 절차

(S. Kato et al., J. Chem. Soc., Perkin Trans. 1997, 1, 3219-3225; J. Smrt et al., Experientia 1957, 15, 291). Crude (R)-methyl 3-hydroxy-2-(N-tritylamino)propanoate (45.20 g, 0.13 mol) was dissolved in CH2Cl2 (300 mL) and cooled to 0° C. under Ar. Methanesulfonyl chloride (10.64 mL, 0.14 mol) was added to the cooled solution, followed by the dropwise addition of Et3N (26.14 mL, 0.19 mol). The resulting solution was allowed to stir at 0° C. (30 min) and then successively washed with 10% aqueous citric acid (200 mL) and saturated aqueous brine (200 mL). After drying (Na2SO4) and evaporation of the solvent, the crude mesylate (53.30 g, 0.12 mol) was dissolved in DME (300 mL) and Et3N (33.73 mL, 0.24 mol) was added. The reaction mixture was stirred at 80° C. (48 h) and then evaporated in vacuo. The residue was dissolved in EtOAc (300 mL) and washed with 10% aqueous citric acid (200 mL) and saturated aqueous brine (200 mL). The organic layer was dried (Na2SO4) and evaporated in vacuo. The crude product was recrystallized (EtOH) to yield 30.81 g (74%) of desired product as a transparent crystal: mp 127-128° C. (Kato, S. et al., J. Chem. Soc., Perkin Trans. 1997, 1, 3219-3225; mp 129-131° C.); [α]20D +94.7° (c 1.5, CHCl3) (Smrt, J. et al., Experientia 1957, 15, 291; [α]20D +95 (c 1, CHCl3)); Rf=0.45 (1/5 EtOAc/hexanes); 1H NMR (CDCl3) δ 1.41 (dd, J=1.7, 6.4 Hz, NCHH′CH), 1.89 (dd, J=2.8, 6.4 Hz, CHH′CHN), 2.26 (dd, J=1.7, 2.8 Hz, NCHH′CH), 3.76 (s, OCH3), 7.20-7.31 (m, 9 PhH), 7.48-7.52 (m, 6 PhH); 13C NMR (CDCl3) δ 28.8 (NCH2CH), 31.8 (CH2CHN), 52.2 (OCH3), 74.5 (NCPh3), 127.1, 127.8, 129.4, 143.7 (3 C6H5), 172.0 (C(O)).

후처리

  1. washsuccessively washed with 10% aqueous citric acid (200 mL) and saturated aqueous brine (200 mL)
  2. customAfter drying
  3. custom(Na2SO4) and evaporation of the solvent
  4. stirringThe reaction mixture was stirred at 80° C. (48 h)
  5. customevaporated in vacuo
  6. dissolutionThe residue was dissolved in EtOAc (300 mL)
  7. washwashed with 10% aqueous citric acid (200 mL) and saturated aqueous brine (200 mL)
  8. dry with materialThe organic layer was dried (Na2SO4)
  9. customevaporated in vacuo
  10. customThe crude product was recrystallized (EtOH)

출처 및 근거

ORD 기록
ord-00a30fe0cf36429c93bfdea2a085d965
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933065B2

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