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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921999Generated: October 30, 2026

Guanidine → HCID 53257950, compound

https://huagongshe.com/reaction/1921999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
ReactantHCID 58336320HCID 58336320—
ProductHCID 53257950HCID 53257950—

Reaction Steps

4-({7-methoxy-3-[2-(methylamino)pyrimidin-4-yl]-1-naphthyl}amino)piperidine-1-carboximidamide was synthesized according to General Procedure A: guanidine formation except 4-(6-methoxy-4-(piperidin-4-ylamino)naphthalen-2-yl)-N-methylpyrimidin-2-amine 150 (0.018 g, 0.050 mmol) was used. The reaction mixture was triturated with ether (10 mL) to obtain 4-({7-methoxy-3-[2-(methylamino)pyrimidin-4-yl]-1-naphthyl}amino)piperidine-1-carboximidamide 204 as a solid (0.007 g). LC/MS (m/z): 406 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173808B2
Source datasetuspto-grants-2012_05
ORD IDord-2adb939e223a42698ecead21b80e24cb
Source noteuspto-grants-2012_05