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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215759Generated: November 1, 2026

Hydrochloric Acid → HCID 21949958, compound

https://huagongshe.com/reaction/2215759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIndole-3-acetamideHCID 397—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 69642170HCID 69642170—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 21949958HCID 2194995838.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A 1.0 M solution of KOtBu in THF (6 mL, 6 mmol) was added to a solution of 2-(1H-indol-3-yl)-acetamide (478 mg, 2.75 mmol) and (1-ethyl-1H-indol-7-yl)-oxo-acetic acid methyl ester (635 mg, 2.75 mmol) in DMF (20 mL). The deep red-orange solution was stirred 12 h at 50° C., allowed to cool, and 1N HCl added. The orange mixture was poured into EtOAc, and the EtOAc layer was separated and washed with 1N HCl, water, saturated NaHCO3 and brine, dried (MgSO4), filtered, and concentrated onto SiO2. Flash chromatography (1:1 EtOAc:hexanes) followed by precipitation from hot methanol afforded the title compound (377 mg, 37%) as a orange-red solid. Heating under vacuum at 70° C. afforded material which was used without further purification. 1H NMR (400 MHz, DMSO-d6) 11.83 (br s, 1H), 11.13 (s, 1H), 7.94 (d, J=3 Hz, 1H), 7.61 (dd, J=8, 1.5 Hz, 1H), 7.3 (m, 2H), 6.93–7.0 (m, 3H), 6.48 (m, 3H), 6.48 (m, 2H), 6.3 (d, J=7 Hz, 1H), 4.0 (m, 2H), 1.06 (t, J=5 Hz, 3H). MS (electrospray, m/z) 354 (M−−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109229B2
Source datasetuspto-grants-2006_09
ORD IDord-c4d714957b604b348e1f07749615d5e3
Source noteuspto-grants-2006_09