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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388282Generated: November 2, 2026

(+-)-3-Quinuclidinol → HCID 13282599, compound

https://huagongshe.com/reaction/1388282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantHCID 13282597HCID 13282597—
ProductHCID 13282599HCID 13282599—

Reaction Steps

The 4-aminobenzil may be prepared according to the method of Augl et al, Annu. Conf., SPE, Reinf. Plastic/Compos. Div. Proc., 26th, 19D, 1 (1971). The 4-aminobenzil is rearranged to yield 4-aminobenzilic acid which is in turn esterfied to produce the ethyl ester. The ethyl ester of the 4-aminobenzilic acid is then reacted with quinuclidin-3-ol to give the expected 3-quinuclidinyl 4-aminobenzilate (4-amino-QNB). The purified 4-amino-QNB is then converted to the 4-triazeno-QNB according to the procedure reported by Tewson et al, J. Nucl. Med. 20, 671 (1979). The purified 4-triazeno-QNB is then reacted with iodide or a desired gamma-emitting radionuclide to produce the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431627
Source datasetuspto-grants-1984_02
ORD IDord-b700dc602e784be89fd368e791ccc348
Source noteuspto-grants-1984_02