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4-Methylmorpholine → N-[(1,1-Dimethylethoxy)carbonyl]-D-alanine 2,5-dioxo-1-pyrrolidinyl ester

HRID 1462115
Notes
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Reaction equation

HRID 1462115 reaction equation
CN1CC[O:5][CH2:4][CH2:3]1.[CH2:8](OC(Cl)=O)[CH:9]([CH3:11])[CH3:10].C([CH2:23][C@H:24]([NH2:28])[C:25]([OH:27])=[O:26])C[C@@H](N)C(O)=O.NC[C:31]([OH:33])=[O:32].C[Si]([CH:38]([Si](C)(C)C)[C:39]([NH2:41])=[O:40])(C)C>ClCCl.CN(C)C=O.C(OC(=O)C)C>[NH:28]([C:31]([O:33][C:9]([CH3:8])([CH3:10])[CH3:11])=[O:32])[C@@H:24]([C:25]([O:27][N:41]1[C:4](=[O:5])[CH2:3][CH2:38][C:39]1=[O:40])=[O:26])[CH3:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 11708267BistrimethylsilylacetamidHCID 87968512meso-DAP (D)GlyOH

Product 1

HCID 11580086N-[(1,1-Dimethylethoxy)carbonyl]-D-alanine 2,5-dioxo-1-pyrrolidinyl ester

Reagents, catalysts & solvents 3

HCID 6228
Dimethylformamide
Solvent
HCID 6344DichloromethaneSolvent2×
HCID 8857Ethyl AcetateSolvent

Procedure

Compound (1) was dissolved in dichloromethane (20 ml.) and N-methyl-morpholine (308 mg.) was added. This solution was cooled in a dry ice-acetone bath (-17°~-19° C.) under stirring, and to the solution, isobutylchlorocarbonate (417 mg.) was added. The reaction mixture was allowed to react for 20 minutes at the same temperature. To the resulting reaction mixture was added to the solution of Compound (2) (1.41 g.) in a mixture of dichloromethane (40 ml.) and N,N-dimethylformamide (4 ml) containing bis (trimethylsilyl)acetamide (3 ml.). The reaction mixture was stirred for 2 hours at -18° C. -10° C. and concentrated under reduced pressure to give an oily residue, which was dissolved in ethylacetate (100 ml.) and washed with 0.5N-Hcl. The organic layer was washed with brine and dried over MgSO4. Evaporation of the solvent gave a white foam which was throughly washed with ether to afford Compound (3) (2.42 g.) as white powder, mp. 145°~149° C. (decomp.)

Workup

  1. temperatureThis solution was cooled in a dry ice-acetone bath (-17°~-19° C.)
  2. customto react for 20 minutes at the same temperature
  3. customTo the resulting reaction mixture
  4. stirringThe reaction mixture was stirred for 2 hours at -18° C. -10° C.
  5. concentrationconcentrated under reduced pressure
  6. customto give an oily residue, which
  7. washwashed with 0.5N-Hcl
  8. washThe organic layer was washed with brine
  9. dry with materialdried over MgSO4
  10. customEvaporation of the solvent
  11. customgave a white foam which
  12. washwas throughly washed with ether

Sources & evidence

ORD record
ord-6559c0c6130249229e6093ec150a32be
Source dataset
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04458078

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes