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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654336Generated: October 30, 2026

Sodium borohydride → Trityllosartan

https://huagongshe.com/reaction/654336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(4'-Methanesulfonyloxymethyl-1,1'-biphenyl-2-yl)-2-triphenylmethyl-2H-tetrazoleHCID 10370839—
ReactantHCID 178418251HCID 178418251—
SolventWaterHCID 962—
ProductTrityllosartanHCID 10865273—

Reaction Steps

To the reaction mixture of Example 10 was added 2-n-butyl-4-chloro-1H-imidazole-5-carboxaldehyde (0.01 m=1.86 g). The reaction was stirred overnight at room temperature. Water (0.87 mL) was added dropwise followed by sodium borohydride pellets (0.37 g). After stirring for 5 hours, the reaction mixture was added slowly to 100 mL water containing 3 mL acetone. The temperature was maintained at about 25° C. during the addition. The resultant slurry was stirred for an additional 45 minutes, then filtered. The solid was rinsed with two 50 mL portions of water. The wet cake was recrystallized first from 50 mL of n-butyl chloride, then from 30 mL of ethyl acetate to give 1.95 g title compound in 28% overall yield; mp 168°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130439
Source datasetuspto-grants-1992_07
ORD IDord-882759e255334b4da66dee61e24b8eee
Source noteuspto-grants-1992_07