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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397779Generated: October 28, 2026

Ammonia → HCID 508581, compound

https://huagongshe.com/reaction/397779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-NitrophenolHCID 980—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 508547HCID 508547—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 508581HCID 50858111%

Reaction Steps

A solution of Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nε-[N′α-(2-thiophenesulfonyl)-L-phenylalanyl]-L-lysine (650 mg, 1.0 mmol, example 24) dissolved in EtOAc (10 mL) was treated with p-nitrophenol (139 mg, 1.0 mmol) and DCC (206 mg, 1.0 mmol) and was left in a refrigerator overnight. Afterwards, the precipitate was filtered off through celite and the solvent evaporated. The crude intermediate was used without further purification in the next step. A portion of the intermediate (25 mg, 0.03 mmol) was added to a solution of ammonia in ethanol (1M, 10 mL). The resulting solution was stirred for 3 h before evaporation of the solvent. The residue was purified by preparative HPLC to yield 2.6 mg, 11% of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610689B2
Source datasetuspto-grants-2003_08
ORD IDord-602d978090f54fab8a3f86a44199d8cf
Source noteuspto-grants-2003_08