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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630580Generated: November 1, 2026

Dimethylbarbituric acid → HCID 60197482, compound

https://huagongshe.com/reaction/1630580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylbarbituric acidHCID 69860—
ReactantHCID 68283605HCID 68283605—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
ProductHCID 60197482HCID 60197482—

Reaction Steps

To a degassed solution of 1-(2-allyl-8-chloro-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-2-pyridin-4-yl-propan-2-ol (300 mg, 0.78 mmol) in DCM (20 mL) were added 1,3-dimethyl barbituric acid (368 mg, 2.3 mmol) and Pd(PPh3)4 (18 mg, 0.015 mmol). After stirring at RT for 30 min, the reaction mixture was diluted with DCM and washed with saturated potassium carbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by reverse phase HPLC to yield 1-(8-chloro-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-2-pyridin-4-yl-propan-2-ol. 1H NMR (CD3OD, formate salt) δ (ppm): 8.4 (d, 2H), 7.48 (d, 2H), 7.4 (s, 1H), 7.18 (d, 1H), 6.98 (d, 1H), 4.6 (bs, 1H), 4.4 (s, 2H), 4.3 (m, 2H), 3.6 (m, 2H), 3.4 (m, 2H), 3.1 (m, 2H). Separation by chiral HPLC provides enantiomers II-62a-b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791132B2
Source datasetuspto-grants-2014_07
ORD IDord-b5426d46cc5c4718babcc332af68ef06
Source noteuspto-grants-2014_07