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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830807Generated: November 1, 2026

Sodium borohydride → Ethyl 4-(3-chlorophenyl)-1,2-dihydro-6-[hydroxy(4-phenyl-2-thiazolyl)methyl]-2-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/1830807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-[(4-phenyl-2-thiazolyl)carbonyl]-3-quinolinecarboxylateHCID 22048464—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(3-chlorophenyl)-1,2-dihydro-6-[hydroxy(4-phenyl-2-thiazolyl)methyl]-2-oxo-3-quinolinecarboxylateHCID 2204846981.7%

Reaction Steps

A mixture of intermediate (18) (0.0336 mol) in methanol (100 ml) and THF (100 ml) was cooled on an ice bath. Sodium tetrahydroborate (0.0336 mol) was added portionwise. The mixture was stirred at a low temperature for 30 min, then poured out into ice water and extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness. The residue was crystallized from 2-propanone/DIPE. The precipitate was filtered off and dried, yielding 14.2 g (81.6%) of ethyl 4-(3-chlorophenyl)-1,2-dihydro-6-[hydroxy(4-phenyl-2-thiazolyl)methyl]-2-oxo-3-quinolinecarboxylate (intermediate 19), mp. 127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067531B2
Source datasetuspto-grants-2006_06
ORD IDord-c43c8d93a0204081b58f580a4abe4591
Source noteuspto-grants-2006_06