HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729607Generated: October 27, 2026
Hydrochloric Acid → HCID 69053768, compound
https://huagongshe.com/reaction/729607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | 1-Chloro-4-nitroisoquinoline | HCID 22765481 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69053768 | HCID 69053768 | 73% |
Reaction Steps
Add NaH (60% in mineral oil, unwashed; 6.23 g, 156 mmol) in portions to a solution of 1-chloro-4-nitroisoquinoline (26.0 g, 125 mmol) and 1-tert-butoxycarbonyl-4-hydroxypiperidine (27.6 g, 137 mmol) in THF (350 mL) stirred at room temperature under nitrogen flow. Stir the dark reddish mixture at 40° C. for 1.5 hours then 55° C. for 1.5 hours. Add additional NaH (1.3 g), and stir the resulting mixture at 55° C. for 2 hours then cool to room temperature overnight. Add hexanes (75 mL), then add water (600 mL) slowly. Adjust the reaction mixture to pH 7 with aqueous HCl (1 N), then separate layers. Discard the aqueous layer and add hexanes (200 mL) to the organic layer. Partially concentrate the mixture under reduced pressure to a volume of 50-100 mL. Add diethyl ether (150 mL) and hexanes (250 mL), then filter the resultant slurry. Wash the cake with diethyl ether/hexanes (1:1) and air-dry to provide 4-(4-nitro-isoquinolin-1-yloxy)-piperidine-1-carboxylic acid tert-butyl ester (33.84 g, 73% yield) as a tan solid. (ES+): m/z 374 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582638B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-d24b7df5c99c44e28cdca157588ecc46 |
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| Source note | uspto-grants-2009_09 |
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