HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912947Generated: October 30, 2026
HCID 178461548, compound → HCID 178461544, compound
https://huagongshe.com/reaction/912947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178461548 | HCID 178461548 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 178461544 | HCID 178461544 | — |
Reaction Steps
To a solution of N-{2-[(2R)-4-(3-chloro-5-hydroxymethyl-pyridin-2-yl)-2-methyl-piperazin-1-yl]-6-trifluoromethyl-3H-benzoimidazol-4-yl}-3,4,5-trifluoro-benzamide (120 mg, 0.2 mmol, Example 170c) in THF (1 mL) was added BH3. THF (0.6 mL, 0.6 mmol, Aldrich) dropwise with stirring at 0° C. The mixture was heated at reflux for 5 h, cooled to room temperature and diluted with 1:1 mixture of MeOH and 1N NaOH (2 mL). The mixture was stirred at room temperature for 30 min and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with brine (10 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography, eluting with 5% MeOH/CH2Cl2 to give the title compound as a white solid. MS (ESI, pos. ion) m/e: 586 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026241B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-45ddf459486c4515a06459549b4f787a |
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| Source note | uspto-grants-2011_09 |
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