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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444155Generated: October 30, 2026

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

https://huagongshe.com/reaction/1444155

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—
ReactantBoc-Ile-Pro-OBzlHCID 14306235—
ProductBoc-D-Tyr(Me)-L-Ile-L-Pro-OBzlHCID 131727885—

Reaction Steps

While cooling on ice, TFA (4 mL) was added to Boc-L-Ile-L-Pro-OBzl (1.00 g, 2.6 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 (6 mL), and Boc-D-Tyr(Me)-OH (770 mg, 2.6 mmol) was added. Then while cooling on ice, HOBt.H2O (597 mg, 3.9 mmol), HBTU (1.50 g, 3.9 mmol), and Et3N (0.88 ml, 6.3 mmol) were added, and the mixture was stirred for 16 hours. The reaction solution was concentrated, and extacted with ethyl acetate. The extract was washed 3 times each with 10% aqueous citric acid solution, 4% aqueous sodium bicarbonate solution, and saturated brine, 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, 0.45 (CHCl3/MeOH, 19/1). Yield: 1.17 g (2.06 mmol, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662778B2
Source datasetuspto-grants-2010_02
ORD IDord-095b40fcad9f4228be433fd905616502
Source noteuspto-grants-2010_02