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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264009Generated: October 26, 2026

4-Methylmorpholine → N-Boc-S-(cyanomethyl)-L-cysteine-L-proline-O-benzyl ester

https://huagongshe.com/reaction/264009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
Reactant(R)-2-((tert-butoxycarbonyl)amino)-3-((cyanomethyl)thio)propanoic acidHCID 22874698—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductN-Boc-S-(cyanomethyl)-L-cysteine-L-proline-O-benzyl esterHCID 131720088—

Reaction Steps

The compound of Example 71 (24.72, 95.06 mmole) and L-proline-O-benzyl ester hydrochloride (22.98 g, 95.06 mmole) are suspended in 140 mL of acetonitrile and 120 mL of DMF at 0° C., then BOP (42.0 g, 95.06 mmole) and NMM (28.84 g, 285.18 mmole) are added. The ice bath is removed after 30 minutes and the reaction is stirred for 18 hours at room temperature. The reaction mixture is reduced in volume under vacuum at 25° C. to give a residue. The residue is taken up in 200 mL ethyl acetate, and is washed successively with 1N hydrochloric acid (1×50 mL) saturated sodium bicarbonate 1×50 mL) and brine (1×50 mL). After drying with MgSO4, the solvent is evaporated under vacuum to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646165
Source datasetuspto-grants-1997_07
ORD IDord-463914f4a5c546c0ae77221e3510a93c
Source noteuspto-grants-1997_07