HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41713Generated: October 28, 2026
Hydrochloric Acid → HCID 66863860, compound
https://huagongshe.com/reaction/41713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 66863357 | HCID 66863357 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66863860 | HCID 66863860 | 92.5% |
Reaction Steps
4-(1′-(tert-Butyl)-1′,2′,3′,4′,5′,6′-hexahydro-3,4′-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester (0.166 g, 0.37 mmol) is placed in 0.65 ml of dichloromethane at 0° C. and then 4N HCl in dioxane (1.4 ml, 5.59 mmol) is added. The reaction medium is stirred at ambient temperature for 18 h. After concentrating to dryness, the reaction medium is hydrolysed with 20 ml of H2O and then K2CO3 is added until a pH of 10 is reached. The aqueous phase is extracted with ethyl acetate. The organic phase is then washed with a saturated aqueous sodium chloride solution, then dried over MgSO4 and concentrated to dryness. 0.12 g of 1-(1′-(tert-butyl)-1′,2′,3′,4′,5′,6′-hexahydro-3,4′-bipyridinyl-6-yl)-1,2,3,4-tetrahydroquinoxaline is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530657B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-a37b78d3b3354be888a4d69d4ef447db |
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| Source note | uspto-grants-2013_09 |
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