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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418422Generated: October 25, 2026

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

https://huagongshe.com/reaction/1418422

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 43 (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 numberUS05883107
Source datasetuspto-grants-1999_03
ORD IDord-b4162a27c0634a2bbe131739664c8af9
Source noteuspto-grants-1999_03