Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-piperidine-1-yl-ethanone | HCID 222312 | — |
| Reactant | HCID 86695580 | HCID 86695580 | — |
| Product | HCID 67518126 | HCID 67518126 | — |
Reaction Steps
Added 2-chloro-1-(piperidin-1-yl)ethanone (50 mg, 0.31 mmol) to a solution of (R)-5-(5-(-(piperidin-3-yl)-1H-1,2,4-triazol-3-yl)-3-(pyridin-4-yl)-1H-indazole (47 mg, 0.106 mmol) and triethylamine (0.3 ml, 2.1 mmol) in MeOH (10 ml). After stirred at 50° C. overnight, reaction mixture was concentrated then purified on preparative TLC (20×20 cm) eluting with 10% v/v MeOH/MeCl2 saturated with NH4OH to yield (R)-1-(piperidin-1-yl)-2-(3-(3-(3-(pyridin-4-yl)-1H-indazol-5-yl)-1H-1,2,4-triazol-5-yl)piperidin-1-yl)ethanone as a white solid (23 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999966B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-0be17eecfcc94316902498b988dd9372 |
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| Source note | uspto-grants-2015_04 |
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