HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173737Generated: October 31, 2026
Hydrochloric Acid → HCID 178507695, compound
https://huagongshe.com/reaction/2173737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Piperidineacetic acid, ethyl ester | HCID 643466 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178507695 | HCID 178507695 | — |
Reaction Steps
NaH (0.234 g, 5.84 mmol) in dry toluene (5 ml) was heated to 80° C. A mixture of acetonitrile (0.229 ml, 4.38 mmol), ethyl 1-piperidineacetate (0.5 g, 2.92 mmol) and toluene (3 ml) was added dropwise to the hot reaction mixture. The mixture was stirred at 80° C. for 1.5 hours and after cooling to RT, quenched by the addition of water (6 ml). Hydrazine hydrate (0.142 ml, 2.92 mmol) was added and reaction mixture reheated to 80° C. for 3 hours. The reaction mixture was acidified with 2N HCl (aq.) to pH 2 and loaded onto a SCX-2 cartridge eluting with MeOH followed by 7M NH3 in MeOH. The methanolic ammonia fractions were concentrated in vacuo to afford an oil. 4N HCl in dioxane (15 ml) was added to the yellow oil and the resulting suspension was filtered and washed with iso-hexane to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056867B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8bc0a6042efa4edbad0a91f1430644a7 |
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| Source note | uspto-grants-2015_06 |
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