HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904400Generated: November 1, 2026
Sodium cyanoborohydride → HCID 54303410, compound
https://huagongshe.com/reaction/1904400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 12857138 | HCID 12857138 | — |
| Reactant | HCID 20038907 | HCID 20038907 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54303410 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837305 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-4c5aecdcb6284f87913444a1c5419a0e |
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| Source note | uspto-grants-1989_06 |
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