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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220408Generated: October 30, 2026

Thioacetamide → HCID 50991652, compound

https://huagongshe.com/reaction/220408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
ReactantHCID 58180534HCID 58180534—
SolventDimethylformamideHCID 6228—
ProductHCID 50991652HCID 509916526.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-(2-chloroacetamido)-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (58.5 mg, 0.141 mmol) in DMF (176 μL) was added thioacetamide (12.71 mg, 0.169 mmol). The vial was capped and the reaction mixture was heated at 80° C. 3 h. The reaction mixture was concentrated in vacuo. The crude residue was taken up in MeOH and purified by prep-HPLC. N,N-Dicyclopropyl-6-ethyl-1-methyl-4-(2-methylthiazol-4-ylamino)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (4.05 mg, 6.6% yield) was isolated as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202881B2
Source datasetuspto-grants-2012_06
ORD IDord-edfa80bd28384ba59b483f65abf8ccd4
Source noteuspto-grants-2012_06