HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775121Generated: October 31, 2026
Hydrochloric Acid → HCID 131734729, compound
https://huagongshe.com/reaction/1775121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Tofacitinib | HCID 9926791 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131734729 | HCID 131734729 | — |
Reaction Steps
A solution of 4M hydrogen chloride in 1,4-dioxane (g, 2.353 mmol) was added to a suspension of tofacitinib free base (0.7 g, 2.24 mmol) in N,N-dimethylformamide (3 mL). The clear solution was stirred at 23 to 25° C. (3 hours) without any solid formation. Ethyl acetate (2 mL) was added and the resulting turbid solution was stirred at room temperature (16 hours) resulting in the formation of a white suspension. An additional portion (5 mL) of ethyl acetate was added and stirring was continued at 23 to 25° C. for 7 hours. The white suspension was filtered, washed with ethyl acetate (2×5 mL) and air-dried for 16 hours to yield tofacitinib hydrochloride (860 mg). 1H NMR analysis showed a molar ratio of tofacitinib hydrochloride to N,N-dimethylformamide of approximately 1:0.8 (14.3 wt %). A PXRD taken of this sample is shown in FIG. 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260438B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-2e770ffdd970432cbefad4df71097f6f |
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| Source note | uspto-grants-2016_02 |
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