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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448585Generated: October 25, 2026

Diisopropylethylamine → 4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid isopropyl ester

https://huagongshe.com/reaction/448585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantIsopropyl 4-aminopiperidine-1-carboxylateHCID 46941577—
Reactant1-(6-Chloropyrimidin-4-yl)-5-(methylsulfonyl)indolineHCID 59566526—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid isopropyl esterHCID 4984878514%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 18b (1.1 g, 5.9 mmol), 6a (1.5 g, 4.84 mmol) and diisopropylethylamine (3 mL, 18.1 mmol) in 15 mL of DMF was heated at 80° C. for 17 h and at 90° C. for 24 h. The mixture was diluted with 100 mL of DCM, washed with brine (3×50 mL) and the extracts were dried, filtered and concentrated under vacuum. The residue was purified by flash chromatography (elution with 50-100% ethyl acetate and 0.1% TEA in hexanes) and finally purified on preparative HPLC to afford 0.3 g (14%) of 18-1. tR=5.21 (Method 5). EC50: 611 nM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481731B2
Source datasetuspto-grants-2013_07
ORD IDord-93eb12c28a2d44f993aaf834adfc9f75
Source noteuspto-grants-2013_07