HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872352Generated: October 30, 2026
HCID 66665648, compound → HCID 66665191, compound
https://huagongshe.com/reaction/872352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66665648 | HCID 66665648 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66665191 | HCID 66665191 | 21.7% |
Reaction Steps
A mixture of (E)-3-{2-[4-(1-amino-cyclobutyl)-phenyl]-3-phenyl-imidazo[1,2-a]pyridin-7-yl}-acrylamide (111 mg, 0.27 mmol) and 10% palladium on carbon (14 mg) in MeOH (10 mL) was stirred under a hydrogen atmosphere for 23 h, additional palladium on carbon (14 mg) was added and the reaction was stirred under a hydrogen atmosphere for 6 h. The resulting mixture was filtered. The resulting solution was concentrated under reduced pressure. The remaining material was purified using MPLC (Biotage Isolera Flash NH2 Snap 10 reverse phase column; 100% CH2Cl2 for 8 min., gradient to 95% CH2Cl2: 5% MeOH over 5 min.; 95% CH2Cl2: 5% MeOH for 4 min., gradient to 80% CH2Cl2: 20% MeOH over 5 min., 80% CH2Cl2: 20% MeOH for 6.2 min.) to give 3-{2-[4-(1-amino-cyclobutyl)-phenyl]-3-phenyl-imidazo[1,2-a]pyridin-7-yl}-propionamide (24 mg, 17%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975265B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a5791e99e8e5475995073f000c50fc7f |
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| Source note | uspto-grants-2015_03 |
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