HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891452Generated: October 30, 2026
HCID 23599479, compound → HCID 23599477, compound
https://huagongshe.com/reaction/891452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23599479 | HCID 23599479 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23599477 | HCID 23599477 | 7.3% |
Reaction Steps
To the solution of (R)-N-(1-azabicyclo[2.2.2]oct-3-yl)(5-(3-cyanophenyl)thiophene-2-carboxamide) (311 mg) in methanol and acetic acid (1:1, 10 mL) a catalytic amount of 10% Pd—C was added and the mixture was hydrogenated at 50 p.s.i. for 36 hr. The mixture was filtered through a pad of celite. The residue was purified first by flash chromatography using 5-20% 3.5M methanolic ammonia chloroform mixtures as the eluent and then by reverse phase HPLC on a Waters Bondapak® C18 column using a gradient of acetonitrile and 0.1% aqueous trifluoroacetic acid as the eluent. The free base was prepared by basification of the product-containing fractions and extraction into chloroform followed by evaporation to gave the title compound (23 mg); MS (ES+) 342 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001914B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-471aac3162d845798c2d012996308d25 |
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| Source note | uspto-grants-2006_02 |
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