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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611099Generated: October 30, 2026

Diisopropylethylamine → HCID 9958698, compound

https://huagongshe.com/reaction/1611099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-Indole-6-carboxaldehydeHCID 2773435—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 11711108HCID 11711108—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 9958698HCID 995869864.3%

Reaction Steps

1H-indole-6-carbaldehyde (238 mg, 1.64 mmol, 1.36 equiv) [Moyer, Mikel P.; Shiurba, John F.; Rapoport, Henry; J. Org. Chem.; 1986, 51, 5106-5110] was added to the solution of the 2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-ylsulfanyl]-N-piperidin-3-ylmethyl-acetamide 1h (TFA)n (1.20 mmol, obtained from step 6) and diisopropylethylamine (0.85 mL, 4.8 mmol, 4 equiv) in 50 mL dichloroethane. Sodium triacetoxyborohydride (0.47 g, 2.24 mmol, 1.8 equiv) was added to the solution and the resulting suspension was stirred vigorously overnight. Methanol (5 mL) was added to quench the reaction. The mixture was concentrated and the residue was diluted with ethyl acetate. The solution was poured into saturated NaHCO3 solution (40 mL) and extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), and concentrated. Chromatography on silica gel (10% methanol in chloroform) afforded 2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-ylsulfanyl]-N-[1-(1H-indol-6-ylmethyl)-piperidin-3-ylmethyl]-acetamide (free base, 410 mg, 64%) as a light tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984643B2
Source datasetuspto-grants-2006_01
ORD IDord-8f6715a2eeea41b2a1fc18a697f1497d
Source noteuspto-grants-2006_01