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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12355Generated: October 23, 2026

N-(3-Aminopropyl)morpholine → 8-Cyclohexyl-2-(3-morpholin-4-yl-propylamino)-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester

https://huagongshe.com/en/reaction/12355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
Reactant8-Cyclohexyl-2-methanesulfonyl-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl esterHCID 25223482—
Product8-Cyclohexyl-2-(3-morpholin-4-yl-propylamino)-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl esterHCID 68583337—

Reaction Steps

Using the procedure outlined in Example 28 Step F, the title compound was prepared from 3-morpholin-4-yl-propylamine and 8-cyclohexyl-2-methanesulfonyl-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (from Example 35 Step E, 20 mg, 0.045 mmol). 8-Cyclohexyl-2-(3-morpholin-4-yl-propylamino)-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester was obtained as a white solid (18 mg, 85%). Mass Spectrum (LCMS, ESI pos.) Calcd. For C23H33N5O4: 444.25 (M+H). Found: 4444.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728003B2
Source datasetuspto-grants-2010_06
ORD IDord-c4849fba64a44787b6809841dc512196
Source noteuspto-grants-2010_06