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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261927Generated: November 3, 2026

1,3-Benzodioxol-5-amine → HCID 66711222, compound

https://huagongshe.com/reaction/1261927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzodioxol-5-amineHCID 84310—
Reactant2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazineHCID 66710791—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 66711222HCID 667112223.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

2-Methane sulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine (67.0 mg, 0.000233 mol) and 1,3-Benzodioxol-5-ylamine (63.9 mg, 0.000466 mol) were dissolved in 2-Methoxyethanol (1.64 mL) and the reaction was heated at 180° C. until HPLC showed consumption of starting material. The reaction mixture was then reduced en vacuo and the product was isolated and purified by Gilson prep HPLC to afford 2.65 mg 1,3-Benzodioxol-5-yl-[7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-amine as a lyophilated powder. (M+H)=361.20. 1H NMR (400 MHz, DMSO, d6) δ 9.29 (s, 1H), 8.93 (s, 1H), 7.75 (d, 1H, J=7.07 Hz), 7.51 (s, 1H), 7.46 (m, 1H), 7.20 (m, 1H), 7.10 (m, 2H), 7.05 (s, 2H), 6.76 (d, 1H, J=8.34 Hz), 5.94 (s, 2H), 3.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-bf60e833282c402ca0e921d0206fbd23
Source noteuspto-grants-2013_06