Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67345319 | HCID 67345319 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67344293 | HCID 67344293 | — |
Reaction Steps
A 4.0 M solution of HCl in 1,4-dioxane (60 ml) was added to 3-(1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (6.11 g, 12.2 mmol) dissolved in 1,4-dioxane (30 ml) at 25° C. The resulting suspension mixture was stirred at 50° C. for 2 h, then was cooled to 25° C. and was concentrated under reduced pressure. Toluene (80 ml) was added to the residue and the mixture was again concentrated under reduced pressure to give crude (1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-yl)-piperidin-3-yl-amine hydrochloride as a yellow solid. This material was used in the next step below without additional characterization or purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461328B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-163e0588eec348cd9f82581c365b9fd9 |
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| Source note | uspto-grants-2013_06 |
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