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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513530Generated: October 31, 2026

Triethylamine → Boc-Leu-Leu-Lys(Z)-OBzl

https://huagongshe.com/reaction/1513530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(S)-2-((S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanamido)-4-methylpentanoic acidHCID 7019882—
ReactantL-Lysine, N6-((phenylmethoxy)carbonyl)-, phenylmethyl ester, hydrochloride (1:1)HCID 11750132—
CatalystAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductBoc-Leu-Leu-Lys(Z)-OBzlHCID 1202054993.6%

Reaction Steps

A solution of H-Lys(Z)—OBzl.HCl (20.35 g, 50 mmol) in DMF (50.0 g) was treated with Et3N (5.26 g, 51 mmol) at 25 to 30° C. Boc-Leu-Leu-OH (17.57 g, 51 mmol) and HOBt (1.08 g, 8 mmol) were added followed by an additional portion of DMF (7.0 g). A solution of DCC (11.35 g, 55 mmol) in DMF (25.0 g) was added dropwise over a period of 30 min at 20° C. The reaction mixture was stirred for 4 h and the temperature was allowed to rise (to ca. 34° C.). Acetic acid (0.2 g) was added, the resulting suspension was filtered and the filter cake was rinsed with DMF (15.0 g). Acetone (126.0 g) was added to the filtrate, followed by two portions of H2O (66.5 g, 89.5 g-30 min apart). The resulting precipitate was filtered and the filter cake was washed with acetone (53.0 g) and H2O (212.0 g). The crude solid was triturated with a mixture of acetone (100 g) and H2O (400 g), filtered, washed with H2O and dried in vacuo at 40° C. to give Boc-Leu-Leu-Lys(Z)—OBzl (32.6 g, 93.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217142B2
Source datasetuspto-grants-2012_07
ORD IDord-cf2584ec478c48229bb19d2aa2dfb6cd
Source noteuspto-grants-2012_07