Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904400Generated: November 1, 2026

Sodium cyanoborohydride → HCID 54303410, compound

https://huagongshe.com/reaction/1904400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 12857138HCID 12857138—
ReactantHCID 20038907HCID 20038907—
SolventMethanolHCID 887—
ProductHCID 54303410HCID 54303410—

Reaction Steps

The title compound was synthesized by the method given for Compound 7 using the following quantities: Compound V (R=1-naphthyl) (0.177 g, 0.5 mmol), 6-oxoheptanoic acid n-butylamide (0.100 g, 0.5 mmol), sodium cyanoborohydride (0.32 g, 0.5 mmol), methanol (2 ml). Purification of a portion of the product after extraction was achieved by semipreparative high pressure liquid chromatography using a C18 column, 1.3 ml/min flow rate with 64% methanol/0.01N hydrochloric acid as eluant. The appropriate fractions were combined, the solvent evaporated under reduced pressure and the residue lyophilized from methanol/water to give 13.8 mg of the hydrochloride salt of the desired compound. The purity of the product was verified by HPLC (1.2 ml/min, 64% methanol/0.01N hydrochloric acid, ret. time=20 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837305
Source datasetuspto-grants-1989_06
ORD IDord-4c5aecdcb6284f87913444a1c5419a0e
Source noteuspto-grants-1989_06