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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986258Generated: October 25, 2026

(Formyloxy)acetonitrile → 2-{5-Chloro-2-[3-(1-formylpiperidin-4-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid cyclopropylamide

https://huagongshe.com/reaction/1986258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Formyloxy)acetonitrileHCID 4205685—
Reactant2-[5-Chloro-2-(3-piperidin-4-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamideHCID 68856919—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-{5-Chloro-2-[3-(1-formylpiperidin-4-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid cyclopropylamideHCID 8662537574.8%

Reaction Steps

Cyanomethyl formate (10 mg, 0.11 mmol) is added to a stirred suspension of 2-[5-chloro-2-(3-piperidin-4-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide (50 mg, 0.11 mmol) in DMF (1 mL) and stirred for 18 hours to form a thick suspension. The mixture is diluted with ethyl acetate (1 mL) then filtered to give the title compound as a solid (41 mg). ES+(m/z) 498 (35Cl) and 500 (37Cl) [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-5ffe8d85ba204466aa5eedb631095487
Source noteuspto-grants-2009_06