Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659642Generated: October 30, 2026

Acetic Acid → HCID 17770045, compound

https://huagongshe.com/reaction/659642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-(Boc-amino)piperidineHCID 4233041—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21087562HCID 21087562—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 17770045HCID 17770045121.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

A 250-mL round-bottomed flask was charged with a solution of 9-(3-(dimethylamino)propyl)-9H-carbazole-3-carbaldehyde (800 mg, 2.86 mmol, 1.00 equiv) in EtOH (120 mL), tert-butyl piperidin-3-ylcarbamate (1.07 g, 5.35 mmol, 1.50 equiv), acetic acid (1.03 g, 17.17 mmol, 6.00 equiv) and NaBH3CN (720 mg, 11.43 mmol, 4.00 equiv). The resulting mixture was stirred at 40° C. in an oil bath for 16 hours. The reaction progress was monitored by TLC (DCM: MeOH=10:1). The reaction was then quenched by the addition of NaHCO3 (50 mL). The mixture was then extracted with dichloromethane (4×50 mL). Combined organic layers were dried over anhydrous sodium sulfate, filtered off and concentrated on a rotary evaporator. The residue was purified by a silica gel column chromatography eluted with dichloromethane/methanol (50/1) affording tert-butyl 14(943-(dimethylamino)propyl)-9H-carbazol-3-yl)methyl)piperidin-3-yl carbamate as brown oil (0.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080566B1
Source datasetuspto-grants-2011_12
ORD IDord-53c40b56fbb9437b8c71922bdeda1b5b
Source noteuspto-grants-2011_12