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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262011Generated: October 28, 2026

Dimethylformamide → 2-(Methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazine-7-carbaldehyde

https://huagongshe.com/reaction/1262011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(Methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazineHCID 57416047—
Reactant7-Bromo-2-(methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazineHCID 57416128—
Product2-(Methylsulfanyl)pyrrolo[2,1-f][1,2,4]triazine-7-carbaldehydeHCID 5741605778.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a cooled (0° C.) mixture of Phosphoryl chloride (55 mL, 0.59 mol) and N,N-Dimethylformamide (27 mL, 0.35 mol) was added 2-Methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine (3.70 g, 0.0224 mol) in N,N-Dimethylformamide (55 mL, 0.71 mol). The addition was added to ensure that the temperature of the reaction stayed below 20° C. After complete addition of 7-Bromo-2-methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine, the mixture was heated at 80° C. and was allowed to stir until HPLC showed consumption of starting material (−1 hour). The reaction was then poured over ice water and was neutralized with saturated sodium bicarbonate. Organics were then extracted with ethyl acetate and combined extracts were dried over magnesium sulfate, filtered and reduced to afford 3.40 g of 2-Methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine-7-carbaldehyde which was used without further purification. 1H NMR (400 MHz, DMSO, d6) δ 10.41 (s, 1H), 9.25 (s, 1H), 7.43 (d, 1H, J=4.96 Hz), 7.05 (d, 1H, J=5.00 Hz), 2.59 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-ee37d4137f0e4684b41f54c8226a2927
Source noteuspto-grants-2013_06