HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41712Generated: October 29, 2026
4-(1'-(tert-Butyl)-1',2',3',6'-tetrahydro-3,4'-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester → HCID 66863357, compound
https://huagongshe.com/reaction/41712
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(1'-(tert-Butyl)-1',2',3',6'-tetrahydro-3,4'-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester | HCID 66863215 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66863357 | HCID 66863357 | 37.6% |
Reaction Steps
4-(1′-(tert-Butyl)-1′,2′,3′,6′-tetrahydro-3,4′-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester (0.44 g, 0.98 mmol) is placed in 60 ml of ethyl acetate in a Parr apparatus bottle. Platinum oxide (0.089 g, 0.39 mmol) is added. After stirring for 4 h under 32 psi H2, the catalyst is filtered off and rinsed with ethyl acetate. The filtrate is concentrated to dryness and then the residue is again stirred in 60 ml of ethyl acetate in the presence of 90 mg of platinum oxide under 35 psi for 18 h. The operation is repeated for 5 h and then 7 h. After filtering off the catalyst and rinsing with ethyl acetate, the filtrate is concentrated and then chromatographed on silica gel, elution being carried out with a methanol/aqueous ammonia gradient in dichloromethane varying from 100/0/0 to 9/1/0.1 (dichloro-methane/methanol/aqueous ammonia). 0.166 g of 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 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-dd5dde13b26d4ac699e8afde692fad4a |
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| Source note | uspto-grants-2013_09 |
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