Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269605Generated: October 31, 2026

1,2-Dichloroethane → HCID 131721926, compound

https://huagongshe.com/reaction/2269605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 131721919HCID 131721919—
SolventDimethylformamideHCID 6228—
ProductHCID 131721926HCID 131721926—

Reaction Conditions

Temperature0 °C

Reaction Steps

Boc-Gly-Pro-Nleu-OH (0.77 g, 2 mmol), HClNH2CH3 (0.27 g, 4 mmol.) and HOBt (0.35 g, 2.5 mmol) were dissolved in DMF and the solution was chilled to 0° C. on a water-ice bath. Triethylamine (0.7 ml) was added slowly while stirring the solution. After 5 minutes, EDC (0.46 g, 2.4 mmol.) was added to the solution and the stirring continued overnight. The DMF was removed under reduced pressure and the resulting mixture was poured into 150 ml chloroform. The chloroform solution was washed by H2O, saturated NaHCO3, brine, saturated NaHSO4 and brine again until the pH of the brine layer was approximate 7. The organic layer was dried using Na2SO4 and the chloroform was distilled under reduced pressure to obtain the Boc-Gly-Pro-Nleu-NHCH3. TLC Rf=0.44 (developing solvents: CMA, 85:15:3). This product was used directly in next step without further purification and characterization. 30 ml solution of 30% TFA in DCM was used to remove the Boc group. The deprotection was allowed to proceed 30 minutes. Then, the DCM and TFA was removed under reduced pressure and benzene 3×20 ml was added and distilled to remove trace TFA. The TFA salt of Gly-Pro-Nleu-NHCH3 was dissolved in 50 ml and the solution was chilled to 0° C. Triethylamine was added slowly to neutralize the peptide. After a while, acetic anhydride (2 ml) was added and the acetylation was allowed to proceed 40 minutes. The DCM was removed and the resulting mixture was dissolved in 100 ml chloroform. The chloroform solution was washed by H2O, saturated NaHCO3, brine, saturated NaHSO4 and brine again until the pH of the brine layer was approximately 7. The organic layer was dried using Na2SO4 and the chloroform was distilled under reduced pressure to obtain the final product Ac-Gly-Pro-Nleu-NHCH3 (0.6 g, 88%). Analytical HPLC profile, single peak, RT=10.5 min. (10-50% B in 30 min.). FAB-MS, observed (M+H)+=341. 1H-NMR (500 MHz, DMSO-d6, 28° C., assignment by TOCSY) δ8.04 (m, C-terminal NH), 7.93 (m, Gly-NH), 7.71 (m, C-terminal NH), 7.48 (m, C-terminal NH), 4.94 (d, Pro-α), 4.81 (m, Pro-α), 4.68 (m, Pro-α), 4.50 (m, Pro-α), 4.29-3.52 (sets of bands, Nleu-α, Gly-α), 3.52-3.42 (m, Pro-δ), 3.36 (m, Pro-δ), 3.29-2.86 (sets of bands, Nleu-β), 2.59 (m, C-terminal N-CH3), 2.53 (m, C-terminal N-CH3), 2.31-2.03 (sets of bands, Pro-β), 1.96 (m, Pro-β, Pro-γ), 1.92-1.61 (m, acetyl-CH3, Pro-β, Nleu-α, Pro-γ), 0.86 (dd, Nleu-δ), 0.75 (m, Nleu-δ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329506B1
Source datasetuspto-grants-2001_12
ORD IDord-fe03974b19da4913bbd8a2e974fbb9db
Source noteuspto-grants-2001_12