1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 67241283, compound

HRID 2384733Notes

Reaction equation

HRID 2384733 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([C:12]([OH:14])=O)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.[CH3:16][O:17][C:18](=[O:22])[CH2:19][CH2:20][NH2:21].C(N(C(C)C)CC)(C)C.CCN=C=NCCCN(C)C.CN(C1C=CC=CN=1)C>ClCCl.C1COCC1>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH:10]([C:12](=[O:14])[NH:21][CH2:20][CH2:19][C:18]([O:17][CH3:16])=[O:22])[CH2:11]1)=[O:7])([CH3:2])([CH3:3])[CH3:4]

Participants

8

Procedure

A solution of azetidine-1,3-dicarboxylic acid mono-tert-butyl ester (0.4 g, 1.98 mmol) and 3-amino-propionic acid methyl ester hydrochloride (0.277 g, 1.98 mmol) in dichloromethane (16 mL) and THF (6 mL) was treated with diisopropylethylamine (0.256 g, 1.98 mmol); it was then added EDCI (0.42 g, 2.18 mmol) and dimethylaminopyridine (0.073 g, 0.59 mmol). The reaction mixture was stirred at room temperature for 50 hours and rotavapored to dryness. The residue was dissolved in dichloromethane. The dichloromethane layer was then successively washed with aqueous 5% citric acid, aqueous saturated hydrogencarbonate solution, brine, dried over Na2SO4, filtered, and the solvent evaporated in vacuo to yield the title compound as a gum (551 mg, 97%).

Workup

  1. washThe dichloromethane layer was then successively washed with aqueous 5% citric acid, aqueous saturated hydrogencarbonate solution, brine
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-b2f4742c12964732b84933a9ec50d1e9
Source dataset
uspto-grants-2012_09
Patent number
US08263781B2

Reaction notes

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