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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435359Generated: October 31, 2026

1-(4-Aminopiperidin-1-yl)ethan-1-one → HCID 21070357, compound

https://huagongshe.com/reaction/1435359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminopiperidin-1-yl)ethan-1-oneHCID 4962477—
ReactantHCID 21070559HCID 21070559—
SolventIsopropanolHCID 3776—
ProductHCID 21070357HCID 21070357—

Reaction Steps

A suspension of (4-amino-2-ethanesulfinyl-pyrimidin-5-yl)-(2-methoxy-5-methyl-phenyl)-methanone (22.3 mg, 0.0698 mmol, Example 325) and 1-(4-amino-piperidin-1-yl)-ethanone (14.9 mg, 0.105 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-methoxy-5-methyl-benzoyl)-pyrimidin-2-ylamino]-piperidin-1-yl]-ethanone as a white solid (23.1 mg). MS (M+H)+, 384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-b213acbd1048480a8102a73ceed2c38a
Source noteuspto-grants-2009_11