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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80768Generated: October 29, 2026

Methanaminium, N-(1-chloroethylidene)-N-methyl-, chloride (1:1) → HCID 86690253, compound

https://huagongshe.com/reaction/80768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanaminium, N-(1-chloroethylidene)-N-methyl-, chloride (1:1)HCID 94113—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178424775HCID 178424775—
SolventDichloromethaneHCID 6344—
ProductHCID 86690253HCID 86690253—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(2,6-dimethylphenyl)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-ol (2.38 g, 6.3 mmol) in DCM (50 mL) at 0° C., was added (1-chloro-ethylidene)-dimethylammonium chloride (Vilsmeier reagent) (2.421 g, 18.91 mmol). The reaction was stirred at 0° C. for 5 min, then at r.t. for 30 min. Saturated aqueous NaHCO3 was added to quench the reaction. The mixture was extracted with DCM three times. The combined organic layers was dried over Na2SO4. After filtration and concentration, the resulting residue was purified via silica gel FCC (0-100% EtOAc/heptane) to give 4-chloro-2-(2,6-dimethylphenyl)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine. 1H NMR (400 MHz, CD2Cl2) δ ppm 7.19-7.27 (m, 1 H), 7.11 (d, J=7.6 Hz, 2 H), 5.80 (s, 1 H), 4.16 (s, 2 H), 3.72 (s, 3 H), 3.32 (t, J=5.9 Hz, 2 H), 3.16 (t, J=5.8 Hz, 2 H), 2.88 (dt, J=13.9, 6.9 Hz, 1 H), 2.11 (s, 6 H), 1.23 (d, J=6.8 Hz, 6 H). MS (ESI+) m/z 396.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846656B2
Source datasetuspto-grants-2014_09
ORD IDord-0dee09621f5c487889f9d1a30779b0c8
Source noteuspto-grants-2014_09