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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017580Generated: October 26, 2026

3-((Tert-butyldimethylsilyl)oxy)propanal → 3-(1-Methylindol-3-yl)-4-[3-(3-tert-butyldimethylsilyloxypropylamino)phenyl]-1h-pyrrole-2,5-dione

https://huagongshe.com/reaction/1017580

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantIron oxide, spentHCID 5327711—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-(1-Methylindol-3-yl)-4-[3-(3-tert-butyldimethylsilyloxypropylamino)phenyl]-1h-pyrrole-2,5-dioneHCID 1201814232%

Reaction Steps

A mixture of 3-(1-methylindol-3-yl)-4-(3-aminophenyl)-1H-pyrrole-2,5-dione (0.2 g, 6 mmol) and 3-(tert-butyldimethylsilyloxy)propionaldehyde (0.25 g, 13 mmol) in CH2Cl2 (10 mL) and MeOH (5 mL) was stirred at room temperature for 15 min and then NaCNBH3 (57 mg, 1.5 eq) was added. The reaction mixture was stirred at RT overnight and then concentrated under vacuo. The residue was purified by preparatory TLC to give 98 mg 3-(1-methylindol-3-yl)-4-[3-(3-tert-butyldimethylsilyloxypropylamino)phenyl]-1H-pyrrole-2,5-dione (32%) MS (LSIMS): (M+H)+ 490, MP: 58-65° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479490B2
Source datasetuspto-grants-2002_11
ORD IDord-4b89cb28b6fd4721a742e1979307e493
Source noteuspto-grants-2002_11