Triethylamine → HCID 178498696, compound

HRID 1425688Notes

Reaction equation

HRID 1425688 reaction equation
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

Participants

7

Reactant 4

HCID 8471Triethylamine2×HCID 31297Methanesulfonyl chlorideHCID 85257MethanesulfonateHCID 7438296Methyl trityl-D-serinate

Product 1

HCID 178498696HCID 178498696, compoundYield 74%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 80711,2-DimethoxyethaneSolvent

Conditions

Temperature
0 °C

Procedure

(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)).

Workup

  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)

Sources & evidence

ORD record
ord-00a30fe0cf36429c93bfdea2a085d965
Source dataset
uspto-grants-2015_01
Patent number
US08933065B2

Reaction notes

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