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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121330Generated: November 3, 2026

Hydrochloric Acid → HCID 22573180, compound

https://huagongshe.com/reaction/2121330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexanoneHCID 7967—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;pyridineHCID 2723995—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 12511560HCID 12511560—
SolventMethanolHCID 887—
ProductHCID 22573180HCID 22573180550.9%

Reaction Steps

To a MeOH (3 mL) solution of 4 Å powdered molecular sieves (0.11 g) under argon is added 3-amino-6,7-dimethoxy-quinoline hydrochloride (0.17 g, 0.68 mmol) and NaOMe (0.039 g, 0.71 mmol). The reaction mixture is stirred at room temperature for 30 min., and cyclohexanone (0.074 mL, 0.71 mmol), then pyridine·borane (0.072 mL, 0.071 mmol) are added portionwise. The mixture is stirred for 4.5 h, then 5N HCl (1.4 mL, 6.8 mmol) is added portionwise. The reaction mixture is stirred 45 min., then made strongly basic with 5N NaOH. The mix is partitioned between EtOAC and H2O, and the aqueous layer is washed with EtOAc (2×). The combined organic layers are washed with brine, (1×), dried (MgSO4), chromatographed (50% EtOAc/hexanes), and recrystallized from EtOAc/hexanes to obtain 0.112 g light-yellow solid in 57% yield (m.p. 164-165). Anal. calcd for C17H22N2O2: C, 71.30; H, 7.74; N, 9.78. Found: C. 71.45; H, 7.49; N, 9.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696434B2
Source datasetuspto-grants-2004_02
ORD IDord-e82bf18e7b4144aba40f53d3a9bc107f
Source noteuspto-grants-2004_02