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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430199Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → [(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/1430199

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantGlycine tert-butyl ester hydrochlorideHCID 2725036—
Reactant3,5-Bis(benzyloxy)picolinic acidHCID 53487995—
Catalyst1-HydroxybenzotriazoleHCID 75771—
SolventDimethylformamideHCID 6228—
Product[(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl esterHCID 5951308399%

Reaction Steps

To a solution of 3,5-bis-benzyloxy-pyridine-2-carboxylic acid, 2, (2.36 g, 6.36 mmol) in DMF (20 mL) at room temperature under N2 is added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI) (1.83 g, 9.54 mmol) and 1-hydroxybenzotriazole (HOBt) (0.086 g, 0.64 mmol). The mixture is stirred for 15 minutes after which time glycine tert-butyl ester hydrochloride (1.60 g, 9.54 mmol) and diisopropylethylamine (DIPEA) (3.32 ml, 19.08 mmol) are added. The resulting solution is stirred at room temperature for 48 hours then concentrated under reduced pressure. The resulting brown oil is purified over silica (EtOAc) to afford 3.04 g (99% yield) of the desired compound as a yellow solid. 1H NMR (250 MHz, CDCl3) δ ppm 8.19 (1H, t, J=5.2 Hz), 8.01-8.08 (2H, m), 7.27-7.54 (9H, m), 6.97 (1H, d, J=2.4 Hz), 5.24 (2H, s), 5.13 (2H, s), 4.17 (2H, d, J=5.2 Hz), 1.51 (9H, s). HPLC-MS: m/z 449 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940773B2
Source datasetuspto-grants-2015_01
ORD IDord-f98ec798819e4a9f85304a675f964219
Source noteuspto-grants-2015_01