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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734665Generated: October 31, 2026

Isopropylamine → HCID 53826697, compound

https://huagongshe.com/reaction/1734665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantHCID 54404171HCID 54404171—
SolventEthanolHCID 702—
ProductHCID 53826697HCID 5382669757%

Reaction Steps

(±)-(1R*, 2S*, 3S*, 5S*)-3-(Acetoxymethyl)-5-(2-bromo-5,6-dichloro-1H-benzimidazol-1-yl)-1,2-cyclopentanediyl diacetate (750 mg, 1.44 mmole) was refluxed in ethanol (10 mL) with isopropylamine (1.22 mL, Aldrich) under nitrogen for 18 hours. A second portion of isopropylamine (1.22 mL) was added and reflux continued for an additional 24 hours. Volatiles were evaporated, the residue was redissolved in ethanol, 1N sodium hydroxide (1.44 mL) was added, and volatiles were reevaporated. The residue was chromatographed on a silica gel column. Title compound was eluted with 10% methanol-chloroform as a colorless glass. The glass was crystallized from ethyl acetate-hexanes to give (±)-(1R*, 2S*, 3S*, 5S*)-5-[5,6-dichloro-2-(isopropylamino)-1H-benzimidazol-1-yl]-3-(hydroxymethyl)-1,2-cyclopentanediol as white crystals (305 mg, 57%); m.p. 213°-214° C.; 1H-NMR(DMSO-d6) identical with that of the enantiomer described in Example 75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534535
Source datasetuspto-grants-1996_07
ORD IDord-f987973663b14683ac4b0d18b85229ee
Source noteuspto-grants-1996_07