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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499057Generated: November 2, 2026

Potassium Phosphate, Tribasic → HCID 67378584, compound

https://huagongshe.com/reaction/1499057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 67373536HCID 67373536—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
ProductHCID 67378584HCID 67378584—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a de-aerated solution of 5-(4-bromo-thiophen-3-yl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (40 mg, 0.111 mmol), phenylboronic acid (20 mg, 0.166 mmol) and K3PO4 (58.8 mg, 0.217 mmol) in DMF-water (4.5:0.5 mL) was added PdCl2(PPh3)2 (3.8 mg, 5 mol %). The reaction mixture was heated at 95° C. for 30 min under nitrogen atmosphere. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford crude material, which was purified by reverse phase HPLC to yield 2,8-dimethyl-5-(4-phenyl-thiophen-3-yl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole as an off white solid (4 mg). 1H NMR (TFA salt, CD3OD) δ (ppm): 7.79-7.65 (m, 2H), 7.3 (s, 1H), 7.2-7.1 (m, 4H), 7.1-7.0 (m, 2H), 6.9 (d, 1H), 4.7 (d, 1H), 4.3 (d, 1H), 3.61-3.60 (m, 1H), 3.25-3.2 (m, 1H), 3.05-3.00 (m, 1H), 2.9 (s, 3H), 2.4 (s, 3H), 2.4-2.39 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199985B2
Source datasetuspto-grants-2015_12
ORD IDord-4c5a48a4cff041a0846c80f985a5b56b
Source noteuspto-grants-2015_12