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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513938Generated: October 30, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 86301334, compound

https://huagongshe.com/reaction/513938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 90417201HCID 90417201—
ReactantHCID 90417207HCID 90417207—
SolventDichloromethaneHCID 6344—
ProductHCID 86301334HCID 8630133467%

Reaction Steps

7-((4-Fluorobenzyl)oxy)-N-methoxy-N-methylquinoline-3-carboxamide. To a solution of 7-((4-fluorobenzyl)oxy)quinoline-3-carbonyl chloride in DCM (14 mL) was added N,O-dimethylhydroxylamine hydrochloride (207 mg, 2.12 mmol) and DIPEA (0.739 mL, 4.23 mmol). The reaction was stirred for 15 minutes at ambient temperature before being concentrated onto silica. Purification (FCC, SiO2, 0-80%, EtOAc/hexanes) afforded the title compound as a white solid (324 mg, 67%). 1H NMR (400 MHz, CDCl3) δ 9.18 (d, J=2.0 Hz, 1H), 8.54 (d, J=1.6 Hz, 1H), 7.81 (d, J=9.0 Hz, 1H), 7.52 (d, J=2.0 Hz, 1H), 7.51-7.44 (m, 2H), 7.32 (dd, J=2.3, 9.0 Hz, 1H), 7.11 (t, J=8.8 Hz, 2H), 5.21 (s, 2H), 3.59 (s, 3H), 3.45 (d, J=0.8 Hz, 3H). [M+H]=341.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102674B2
Source datasetuspto-grants-2015_08
ORD IDord-316ab5691eda487fb77fa2fc05a1ba2d
Source noteuspto-grants-2015_08