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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363207Generated: October 30, 2026

Dimethylformamide → HCID 67705207, compound

https://huagongshe.com/reaction/363207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantHCID 86751188HCID 86751188—
SolventEthyl AcetateHCID 8857—
ProductHCID 67705207HCID 67705207—

Reaction Steps

To a solution of 2(R and S)-[1-(t-butoxycarbonyl)-pyrrolidin-2(S)-ylmethyloxy]-3-phenylpropionic acid (263.6 mg, 0.754 mmol) in DMF (8.0 mL) were added 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (HOOBT, 137 mg, 0.840 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 164 mg, 0.855 mmol), L-methionine methyl ester hydrochloride (176 mg, 0.881 mmol), and Et3N (0.35 mL, 2.5 mmol). The reaction was stirred under argon at ambient temperature for 18 h, diluted with EtOAc (70 mL), and washed with 10% aq citric acid (70 mL), saturated aq NaHCO3 (40, 20 mL), and saturated aq NaCl (40 mL). The organic layer was dried (Na2SO4) and evaporated in vacuo. The diastereomeric crude products were purified and separated by chromatography (silica gel, 1:19 to 1:2 EtOAc/CH2Cl2) to give the title compound. 1H NMR (CD3OD, 400 MHz) δ7.35-7.17 (m, 5H), 4.63-4.55 (m, 1H), 4.08-3.90 (m, 2H), 3.72 (s, 3H), 3.55-3.46 (m, 2H), 3.34-3.22 (m, 1H), 3.09 (dd, J=14, 4 Hz, 1H), 2.91 (dd, J=14, 7 Hz, 1H), 2.38-2.20 (m, 2H), 2.10-2.00 (m, 1H), 2.04 (br s, 3H), 1.97-1.86 (m, 6H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872135
Source datasetuspto-grants-1999_02
ORD IDord-0316b099d24449feafd56746afc5d309
Source noteuspto-grants-1999_02