HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469409Generated: October 30, 2026
Bms-973013 → 4-(3,4-Dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-2-[4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidin-1-yl]-benzonitrile
https://huagongshe.com/reaction/469409
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bms-973013 | HCID 22293182 | — |
| Reactant | 4-(3,4-Dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-2-fluoro-benzonitrile | HCID 58181089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3,4-Dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-2-[4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidin-1-yl]-benzonitrile | HCID 25271154 | — |
Reaction Steps
0.26 g (1.2 mmol) 1-piperidin-4-yl-1,3-dihydroimidazo[4,5-b]pyridin-2-one and 93 mg (0.30 mmol) 4-(3,4-dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-2-fluoro-benzonitrile were combined and heated to 300° C. for approx. 10 min. Then the mixture was dissolved in DMF and purified by preparative HPLC-MS. The fractions containing the product were combined and the organic solvent was evaporated down. The residue was neutralised with 1N aqueous sodium hydroxide solution, the precipitate formed was suction filtered, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629137B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-20de981dacc4436c8c382f6dde0e97b0 |
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| Source note | uspto-grants-2014_01 |
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