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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014309Generated: October 31, 2026

Hydrazine hydrate (1:1) → 2-[(Dimethylamino)acetyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-isoquinolinamine

https://huagongshe.com/reaction/1014309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN,N-dimethyl-2-[6-(methyloxy)-7-nitro-3,4-dihydro-2(1H)-isoquinolinyl]-2-oxoethanamineHCID 59441912—
CatalystIron chloride (FeCl3)HCID 24380—
SolventMethanolHCID 887—
Product2-[(Dimethylamino)acetyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-isoquinolinamineHCID 5944192826.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

A suspension of N,N-dimethyl-2-[6-(methyloxy)-7-nitro-3,4-dihydro-2(1H)-isoquinolinyl]-2-oxoethanamine (0.9 g, 3.07 mmol), hydrazine hydrate (0.67 mL, 21.5 mmol), iron(III)chloride (0.125 g, 0.77 mmol), activated carbon (1 g), and methanol (100 mL) was maintained at 65° C. for 12 hours, cooled, and filtered through celite (rinsed with additional methanol). Filtrates were concentrated, redissolved in ethyl acetate, and washed twice with saturated aqueous sodium chloride and sodium bicarbonate. The organic layer was dried over sodium sulfate, filtered, and concentrated to afford 2-[(dimethylamino)acetyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-isoquinolinamine (0.214 g, 26%) as a white solid. 1H NMR/80° C. (400 MHz, DMSO-d6) δ ppm 6.56 (s, 1 H), 6.41 (s, 1 H), 4.49 (s, 2 H), 4.38 (s, 2 H), 3.73 (3.64 (s, 2 H), 3.11 (s, 2 H), 2.66 (s, 2 H), 2.20 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-a874cc1b44744c5d88a7cd8d1aa35af9
Source noteuspto-grants-2011_07