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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779503Generated: October 31, 2026

1,2-Dichloroethane → HCID 22872485, compound

https://huagongshe.com/reaction/1779503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantHCID 22872482HCID 22872482—
SolventEthyl AcetateHCID 8857—
ProductHCID 22872485HCID 2287248575.7%

Reaction Conditions

Temperature23 °C

Reaction Steps

N-[(tert-Butyloxy)carbonyl-3(S)-ethylpyrrolidin-2(S)-ylmethyl]-proline (0.238 mmol), HOBT (0.048 g, 0.262 mmol), EDC (0.068 g, 0.0357 mmol), and methionine methyl ester hydrochloride (0.048 g, 0.238 mmol) were dissolved in CH2CL2 (10 mL) and stirred at 23° C. for 18 h. EtOAc (100 mL) was added, and the mixture washed with satd NaHCO3 solution, H2O, brine, and dried (MgSO4). Filtration and concentration to dryness gave 0.085 g of title compound. 1H NMR (CD3OD) δ(major rotamer) 4.63 (t, 1H, J=7 Hz), 3.73 (s, 3H), 3.55-3.7 (m, 1H), 3.0-3.5 (m,4H), 2.3-2.7 (m, 5H), 1.9-2.2 (m, 3H), 2.08 (s, 3H), 1.6-1.9 (m, 4H), 1.46 (s, 9H), 1.3-1.45 (m, 2H), 0.92-1.02 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627202
Source datasetuspto-grants-1997_05
ORD IDord-fa17f4afafd7426d967c69d4be9f6f61
Source noteuspto-grants-1997_05