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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090455Generated: October 30, 2026

Hydrochloric Acid → HCID 59402369, compound

https://huagongshe.com/reaction/2090455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59402292HCID 59402292—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 59402369HCID 5940236987.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

tert-butyl 3-methyl-7-(1-methyl-1H-pyrazol-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (0.320 g, 0.977 mmol) in ethyl acetate (1 mL) was treated with 4.0 M of hydrogen chloride in 1,4-dioxane (1.00 mL, 4.00 mmol) at r.t. for 1 h. The mixture was diluted with ether (5 mL), and was centrifugalized. The solvents were decanted. The residue was dried in-vacuo, and dissolved in tert-butanol (10 mL). To the solution was added 2-amino-4,6-dichloropyrimidine (0.246 g, 1.50 mmol) and N,N-diisopropylethylamine (522 uL, 3.00 mmol). The mixture was heated and stirred at 120° C. overnight. The solvent was removed under reduced pressure. The residue was purified by flash chromatography on a silica gel column with methanol in DCM (0-10%) to give the desired product (303 mg, 87.6%). LCMS (M+H)+: m/z=355.1/357.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436008B2
Source datasetuspto-grants-2013_05
ORD IDord-846e779d95094d619fcb21f13773b62a
Source noteuspto-grants-2013_05