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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526427Generated: November 3, 2026

N-Methyl-D-glucamine → (R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid N-methylglucamine salt

https://huagongshe.com/reaction/1526427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-D-glucamineHCID 8567—
Reactant(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acidHCID 53362086—
SolventAcetoneHCID 180—
Product(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid N-methylglucamine saltHCID 53378134—

Reaction Conditions

Temperature50 °C

Reaction Steps

(R)-2-(9-Chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid (15 mg, 0.0311 mmol) was dissolved in acetone (0.5 mL) and warmed to 50° C. Aqueous N-methylglucamine (14 uL, 2.27M) was added and the mixture was allowed to slowly cool to 30° C. over 24 h. The reaction mixture was evaporated to dryness, and EtOAc (0.5 mL) was added to provide a solid which was collected by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085581B2
Source datasetuspto-grants-2015_07
ORD IDord-79a6ebd51e3f4b17a7fb05440a1d296a
Source noteuspto-grants-2015_07