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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444157Generated: October 31, 2026

Water → Boc-D-Tyr(Me)-L-Ile-D-Pro-OBzl

https://huagongshe.com/reaction/1444157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantBoc-O-methyl-D-tyrosineHCID 7017908—
ReactantHCID 58726192HCID 58726192—
ProductBoc-D-Tyr(Me)-L-Ile-D-Pro-OBzlHCID 58726683—

Reaction Steps

While cooling on ice, TFA (5 mL) was added to Boc-L-Ile-D-Pro-OBzl (1.63 g, 3.38 mmol), and this was left to stand for 30 minutes. TFA was removed by evaporation, and the residue was dried under reduced pressure. This was dissolved in DMF (8 mL), Boc-D-Tyr(Me)-OH (1.50 g, 5.07 mmol) was added, and while cooling on ice, HOBt.H2O (518 mg, 3.38 mmol), HBTU (1.92 g, 5.07 mmol), and Et3N (2.37 ml, 16.9 mmol) were added, and this mixture was stirred for 3 hours. The reaction solution was concentrated, extracted with ethyl acetate, the extract was washed 3 times each with 10% aqueous citric acid solution, 4% aqueous sodium bicarbonate solution, and saturated bee, and dried over magnesium sulfate, and then ethyl acetate was removed by evaporation. Purification by silica gel chromatography yielded the desired product as a foam (column: Merck Kieselgel 60 Φ 3.4×30 cm, eluent: CHCl3/MeOH, 99/1). TLC: Rf, 0.89 (CHCl3/MeOH, 9/1). Yield: 1.44 g (2.42 mmol, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662778B2
Source datasetuspto-grants-2010_02
ORD IDord-80c4e58623cb41e9809103b5ba8815df
Source noteuspto-grants-2010_02