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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414001Generated: October 31, 2026

4-Methylmorpholine → Fmoc-Lys(Alloc)-Glu(OtBu)-Arg(Pmc)-Val-Asp(OAllyl)-OBzl

https://huagongshe.com/reaction/414001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPyBOPHCID 2724699—
Reactant(2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-6-(((prop-2-en-1-yloxy)carbonyl)amino)hexanoic acidHCID 11123257—
ReactantGlu(OtBu)-Arg(Pmc)-Val-Asp(Allyl)-OBzlHCID 178459569—
SolventAcetonitrileHCID 6342—
ProductFmoc-Lys(Alloc)-Glu(OtBu)-Arg(Pmc)-Val-Asp(OAllyl)-OBzlHCID 17845956774.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A suspension of Fmoc-Lys(Alloc) (4.2 g, 9.3 mmol) and benzotriazolyloxy-tris[pyrrolidino]-phosphonium hexafluoroacetate (PyBOP, 4.8 g, 9.3 mmol) in 69 mL acetonitrile at 5° C. is treated with N-methylmorpholine (0.94 g, 9.3 mmol), resulting in formation of a solution which is stirred at 5° C. for 30 minutes. A suspension of Glu(OtBu)-Arg(Pmc)-Val-Asp(Allyl)-OBzl (9 g, 9.3 mmole) in 52 mL acetonitrile is added, causing the reaction mixture to become cloudy white. N-methylmorpholine is added until the reaction mixture is at pH 7, then the mixture is allowed to warm to ambient temperature and stir for 1.33 hours. The mixture is filtered and the solid residue is washed with acetonitrile (2×40 mL) and dried overnight under vacuum with a nitrogen bleed to give 12.8 g of an off-white crusty solid which is triturated with 200 mL methyl-t-butyl ether, collected by filtration and dried under vacuum to afford 9.7 g of Fmoc-Lys(Alloc)-Glu(OtBu)-Arg(Pmc)-Val-Asp(OAllyl)-OBzl. (SEQ ID NO: 39) (Mcalc 1404.7; M+1obsvd 1406).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569993B1
Source datasetuspto-grants-2003_05
ORD IDord-f95b68c7c7fd4944a1a1171bb79be862
Source noteuspto-grants-2003_05