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Sodium Iodide → Glycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl ester

HRID 1110304
Notes
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Reaction equation

HRID 1110304 reaction equation
[C:1]([CH2:4][N:5](C1C=C(OCCCCCCCCCC)C=C(OCCCCCCCCCC)C=1)CC(O)=O)(O)=[O:2].C(N(CC)C(C)C)(C)C.[NH:47]([CH2:51][CH2:52][OH:53])[CH2:48][CH2:49][OH:50].Cl[CH2:55][C:56](Cl)=[O:57].C(N(CC)CC)C.[I-].[Na+].CN(C=[O:72])C>>[OH:50][CH2:49][CH2:48][N:47]([CH2:55][CH2:56][OH:57])[C:51]([CH2:52][O:53][C:1](=[O:2])[CH2:4][NH2:5])=[O:72]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 5238Sodium IodideHCID 6228DimethylformamideHCID 6577Chloroacetyl chlorideHCID 8113DiethanolamineHCID 8471TriethylamineHCID 81531DiisopropylethylamineHCID 192621N-(carboxymethyl)-N-(3,5-bis(decyloxy)-phenyl)glycine

Product 1

HCID 131718524Glycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl ester

Procedure

A mixture of 1.0 g (1.92 mmol) of N-(carboxymethyl)-N-[3,5-bis(decyloxy)phenyl]glycine, 2.6 ml of N,N-diisopropylethylamine and a solution of N,N-bis(2-hydroxyethyl)-3-chloroacetamide [prepared from the reaction of 2.1 g (20 mmol) of diethanolamine, 1.6 ml (20 mmol) of chloroacetyl chloride and 3.1 ml (22 mmol) of triethylamine in 25 ml of DMF] was stirred at room temperature for 17 hours. Sodium iodide (3.0 g, 20 mmol) was added and the reaction mixture was stired and heated at 60° under argon for 25 hours. The mixture was concentrated at reduced pressure and NaHCO3 solution was added to the residue. The product was extracted with ethyl acetate and the extract was washed with water, dried and concentrated to an oil which was crystallized from methylene chloride-ether to give 0.455 g (29% yield, mp 104°-107°) of N-[3,5-bis(decyloxy)phenyl]-N-[[bis(2-hydroxyethyl)amino]carbonyl]methoxy]-2-oxoethyl]glycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl ester.

Workup

  1. temperatureheated at 60° under argon for 25 hours
  2. concentrationThe mixture was concentrated at reduced pressure and NaHCO3 solution
  3. additionwas added to the residue
  4. extractionThe product was extracted with ethyl acetate
  5. washthe extract was washed with water
  6. customdried
  7. concentrationconcentrated to an oil which
  8. customwas crystallized from methylene chloride-ether

Sources & evidence

ORD record
ord-b9e678ea41a84d989f5f2f0748458c06
Source dataset
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05324747

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes