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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21308Generated: October 26, 2026

Acetic Acid → 4-Methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-(pyrrolidin-1-ylmethyl)indol-2-yl]isoindolinone

https://huagongshe.com/reaction/21308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-formylindol-2-yl]isoindolinoneHCID 86628325—
SolventAcetonitrileHCID 6342—
Product4-Methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-(pyrrolidin-1-ylmethyl)indol-2-yl]isoindolinoneHCID 8662832835.3%

Reaction Steps

In a similar manner to Step 2 of Example 6, 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-formylindol-2-yl]isoindolinone (0.299 g, 0.597 mmol) was dissolved in acetonitrile (15.0 mL), and the solution was treated with pyrrolidine (0.997 mL, 11.9 mmol), acetic acid (0.684 mL, 11.9 mmol) and sodium triacetoxyborohydride (0.633 g, 2.99 mmol), followed by purification of the residue by flash column chromatography (chloroform/methanol=3/1) to obtain 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-(pyrrolidin-1-ylmethyl)indol-2-yl]isoindolinone (0.117 g, yield 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-d7f028aefaa048da87fa397fcb3af310
Source noteuspto-grants-2010_06