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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435217Generated: November 1, 2026

1-(4-Aminopiperidin-1-yl)ethan-1-one → HCID 10092678, compound

https://huagongshe.com/reaction/1435217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminopiperidin-1-yl)ethan-1-oneHCID 4962477—
ReactantHCID 21070569HCID 21070569—
SolventIsopropanolHCID 3776—
ProductHCID 10092678HCID 10092678—

Reaction Steps

A suspension of (4-amino-2-ethanesulfonyl-pyrimidin-5-yl)-(2,6-difluoro-3-methoxy-phenyl)-methanone (20.0 mg, 0.056 mmol, Example 89) and 1-(4-amino-piperidin-1-yl)-ethanone (21.1 mg, 0.148 mmol, prepared as described in U.S. Pat. No. 5,817,828) in isopropyl alcohol (2.5 mL) was heated at 120° C. in a sealed tube under microwave conditions for 0.3 to 1 hour. The resulting reaction mixture was evaporated in vacuo and crude product was purified on silica gel with 95:5 of dichloromethane/methanol to give 1-[4-[4-amino-5-(2,6-difluoro-3-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidin-1-yl]-ethanone as a white solid (18.3 mg). MS (M+H)+, 406.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-b281f98f2af84b81a87a208049a605fc
Source noteuspto-grants-2009_11