HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050608Generated: October 29, 2026
Hydrochloric Acid → HCID 118115143, compound
https://huagongshe.com/reaction/1050608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 118115261 | HCID 118115261 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 118115143 | HCID 118115143 | — |
Reaction Steps
(R)-tert-Butyl 3-aminopiperidine-1-carboxylate (1.70 g, 8.5 mmol) was mixed with p-anisic acid (1.42 g, 9.35 mmol) in 5 mL DMF and 25 mL dioxane. The mixture was stirred at RT, and to it were added DIEA (2.07 mL, 11.9 mmol) and then PyBOP (4.86 g, 9.35 mmol). The mixture was stirred at RT for 3 hours, diluted with 150 mL EtOAc, washed with water 60 mL×3, dried, concentrated, subjected to silica flash column using 0 to 20% EtOAc in DCM to isolate (R)-tert-butyl 3-(4-methoxybenzamido)piperidine-1-carboxylate (488) in quantitative yield. Compound 488 (1.86 g, 5.56 mmol) was treated with 30 mL commercial 4N HCl in dioxane at RT for 15 min, giving (R)-4-methoxy-N-(piperidin-3-yl)benzamide hydrochloride (489) in quantitative yield as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382246B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-b89f362f5ddc432e9cb3b3d34f2ef457 |
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| Source note | uspto-grants-2016_07 |
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