HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41208Generated: October 28, 2026
HCID 86672430, compound → HCID 86672429, compound
https://huagongshe.com/reaction/41208
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86672430 | HCID 86672430 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86672429 | HCID 86672429 | 50% |
Reaction Steps
A solution of tert-butyl 2-(6-(dimethylcarbamoyl)-2-morpholino-4-oxo-4H-chromen-8-yl)-1H-pyrrole-1-carboxylate (0.6 g, 1.28 mmol) in MeOH (10 mL) was hydrogenated over 5% Rh/Al2O3 (NanoThales CatCart cartridge, product ID THS 02118) with the H-Cube (Continuous flow hydrogenation apparatus HC-2.5S from THALES Nanotechnology Inc. Budapest H-1031; Zahony u.7.; Hungaria) at 10 bars, 50° C. and a flow rate of 1 mL/min. for 3.5 h with continuous recycling. The cartridge was replaced by a 10% Pd/c cartridge and hydrogenation was pursued for 6 h at 60 bars and 60° C. The mixture was evaporated to dryness to give a solid which was triturated in diethyl ether, filtered and dried under vacuum at 50° C. to afford pure tert-butyl 2-(6-(dimethylcarbamoyl)-2-morpholino-4-oxo-4H-chromen-8-yl)pyrrolidine-1-carboxylate (0.30 g, 50%) as a white solid. The crude product was used as such for the next step. Mass Spectrum: m/z [M+H]+=472.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530470B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-036c2f16253e409392004d8e2fe6cc80 |
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| Source note | uspto-grants-2013_09 |
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