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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11865Generated: October 25, 2026

Nitrate → HCID 178418760, compound

https://huagongshe.com/reaction/11865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrateHCID 943—
ReactantTriethylamineHCID 8471—
Reactant(S)-2-((4-aminomethylbenzoyl)amino)-5-(N-Boc-2-picolylaminomethyl)valeric AcidHCID 21043758—
SolventDimethylformamideHCID 6228—
ProductHCID 178418760HCID 178418760—

Reaction Steps

The compound obtained in Example 41-5 (0.01 g) was dissolved in DMF (0.3 ml). After the addition of dimethylpyrazolecarboxyamidine nitrate (0.01 g), the mixture was adjusted to pH 8 with triethylamine and stirred for 3 days. The reaction solution was concentrated. Chloroform was added to the residue and the mixture was washed with saturated aqueous solution of sodium hydrogencarbonate. The organic layer was concentrated and dried under reduced pressure. The residue was purified by silica gel column chromatography (5 g, chloroform/methanol/water=7/3/0.5) to obtain the title compound (0.01 g) as white foam. The foam was dissolved in methanol (0.3 ml) and 4 mol/l hydrochloric acid/dioxane solution (0.3 ml) was added dropwise. The mixture was stirred for 3 hours at room temperature. The reaction solution was concentrated and dried under reduced pressure to obtain a crude product (0.01 g). The crude product was purified by silica gel column chromatography (0.5 g, chloroform/methanol/water=7/3/0.5) and 1 mol/l hydrochloric acid was added. The mixture was concentrated to obtain hydrochloride of the title compound (0.01 g) as white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098215B2
Source datasetuspto-grants-2006_08
ORD IDord-1b8da72fa0b543b09dd1bd7a4a052cdb
Source noteuspto-grants-2006_08