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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205243Generated: October 30, 2026

Methyl iodide → HCID 178430231, compound

https://huagongshe.com/reaction/2205243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178430232HCID 178430232—
SolventDimethylformamideHCID 6228—
ProductHCID 178430231HCID 17843023126.1%

Reaction Steps

To a solution of trans-4-(3-(7-methylthieno[3,2-c]pyridin-2-yl)imidazo[1,2-b]pyridazin-6-ylamino)cyclohexanol (37 mg, 0.0975 mmol, 1.0 equiv) in DMF (2.00 mL) was added sodium hydride (20 mg, 0.488 mmol, 5.0 equiv) and methyl iodide (68 mg, 0.488 mmol, 5.0 equiv). After 2 h, the reaction mixture was quenched with water and extracted with ethyl acetate. Purification by column chromatography gave 20 mg (50%) of N-((1r,4r)-4-methoxycyclohexyl)-N-methyl-3-(7-methylthieno[3,2-c]pyridin-2-yl)imidazo[1,2-b]pyridazin-6-amine as the less polar product and 10 mg (25%) of trans-4-(N-methyl-N-(3-(7-methylthieno[3,2-c]pyridin-2-yl)imidazo[1,2-b]pyridazin-6-yl)amino)cyclohexanol as the more polar product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09370515B2
Source datasetuspto-grants-2016_06
ORD IDord-b6927ab0505d42278d82dfb53fcfa1cd
Source noteuspto-grants-2016_06