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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526424Generated: November 3, 2026

Tris(hydroxymethyl)aminomethane → (R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid 2-amino-2-hydroxymethyl-propane-1,3-diol

https://huagongshe.com/reaction/1526424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
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—
SolventEthyl AcetateHCID 8857—
Product(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid 2-amino-2-hydroxymethyl-propane-1,3-diolHCID 53378131—

Reaction Conditions

Temperature60 °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 EtOAc (0.5 mL) and warmed to 60° C. Aqueous 2-amino-2-hydroxymethyl-propane-1,3-diol (TRIS, 8.0 uL, 4.0 M) was added. The reaction mixture was allowed to cool to room temperature over 24 h and the solids were collected by filtration. The PXRD pattern of the title compound is shown in FIG. 13; and the DSC and TGA are shown in FIG. 14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085581B2
Source datasetuspto-grants-2015_07
ORD IDord-20e366e471cd4761b7df0d0c278a3712
Source noteuspto-grants-2015_07