HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044460Generated: November 3, 2026
Sodium Bicarbonate → HCID 68515995, compound
https://huagongshe.com/reaction/1044460
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 87481919 | HCID 87481919 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 68515995 | HCID 68515995 | — |
Reaction Steps
To a solution of n-BuLi (1.6 M in hexane, 2.22 mL, 3.56 mmol) in THF (10 mL), maintained at 0° C. under nitrogen atmosphere, hexamethyldisilazane (0.74 mL, 3.56 mmol) was added dropwise and stirred for 15 min. To this, a solution of the compound of example (59)(0.95 g, 1.78 mmol) in THF (5 mL) was added drop wise, maintaining the temperature at 0° C. After the addition, the reaction was allowed to warm to room temperature and stirred for 2.5 hrs. The reaction mixture was acidified with dilute HCl, and basified with 10% sodium bicarbonate to pH 8-9. The aqueous layer was extracted with chloroform (3×50 mL). The organic layer was washed with water (25 mL), brine (25 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated under reduced pressure and dried under vacuum to yield acetic acid 3-{3-[3-(2-chloro-4-isopropylamino-phenyl)-3-oxo-propionyl]-2-hydroxy-4,6-dimethoxy-phenyl}-1-methyl-pyrrolidin-2-ylmethyl ester as a brown solid (0.95 g). This ester was dissolved in conc. HCl (5 mL) and stirred for 3 hrs. to effect cyclisation. At the end of 3 hrs, the reaction mixture was basified with solid NaHCO3 to pH 8-9. The aqueous layer was extracted with chloroform (3×25 mL) and washed with water (10 mL) and brine (10 mL). The organic layer was dried over anhydrous Na2SO4, concentrated under reduced pressure and dried over vacuum to yield the compound, (+)-trans-2-(2-chloro-4-isopropylaminophenyl)-8-(2-hydroxy methyl-1-methylpyrrolidin-3-yl)-5,7-dimethoxy-chromen-4-one, as a brown solid which was taken ahead without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563596B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-5dd007b3b6fb487c8e7451d8f634e8d9 |
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| Source note | uspto-grants-2013_10 |
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