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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170859Generated: October 27, 2026

1H-Indole-5-Carboxylic Acid → HCID 67168639, compound

https://huagongshe.com/reaction/2170859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant4-(4-Chlorophenoxy)piperidine hydrochlorideHCID 17749791—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67168639HCID 6716863994%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 4-(4-chlorophenoxy)piperidine hydrochloride (300 mg, 1.21 mmol), 1H-indole-5-carboxylic acid (195 mg, 1.21 mmol), and N,N-diisopropylethylamine (0.85 mL, 4.84 mmol) in N,N-dimethylformamide (10 mL) was add HBTU (688 mg, 1.81 mmol) at room temperature. After stirring at 60° C. for 2 hours, the mixture was poured into water (50 mL). This was extracted with ethyl acetate (50 mL) and washed with water (50 mL). The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (NH-gel, eluting with n-hexane/ethyl acetate=1/1) to give 403 mg (94% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051296B2
Source datasetuspto-grants-2015_06
ORD IDord-5a3196fa23304d54ad69491addb8b8f3
Source noteuspto-grants-2015_06