HuagongsheHuagongshe Chemistry Print Report · For research reference only
(+-)-3-Quinuclidinol → HCID 13282599, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (+-)-3-Quinuclidinol | HCID 15381 | — |
| Reactant | HCID 13282597 | HCID 13282597 | — |
| Product | HCID 13282599 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04431627 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-b700dc602e784be89fd368e791ccc348 |
| Source note | uspto-grants-1984_02 |