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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696836Generated: November 1, 2026

Potassium Carbonate → [4-(4-{4-[2-(4-Benzyloxy-3-formylaminophenyl)-2-(R)-hydroxyethylamino]pentyl}-phenyl)butyl]carbamic acid benzyl ester

https://huagongshe.com/reaction/1696836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-N-[5-(2-Bromo-1-hydroxyethyl)-2-(phenylmethoxy)phenyl]formamideHCID 11142645—
Reactant{4-[4-(4-Aminopentyl)phenyl]butyl}carbamic acid benzyl esterHCID 58100158—
SolventChloroformHCID 6212—
Product[4-(4-{4-[2-(4-Benzyloxy-3-formylaminophenyl)-2-(R)-hydroxyethylamino]pentyl}-phenyl)butyl]carbamic acid benzyl esterHCID 86649686—

Reaction Steps

A suspension composed of compound 26 (0.59 g, 1.60 mmol), compound 5 (0.42 g, 1.19 mmol); K2CO3 (0.23 g, 1.68 mmol) and chloroform (25 mL) was heated to reflux for 72 h, then cooled to ambient temperature. The solid was vacuum filtered and washed with chloroform (3×10 mL). The filtrate and the washings were combined and concentrated. The residue was subjected to column chromatography eluting with 0-10% methanol in dichloromethane. The un-reacted starting material 26 (0.39 g; 66% recovery) was recovered in the separation. A mixture of two diastereomers of the desired products 27, which were not separable in this step, was obtained (0.29 g, 28%) as a colorless, viscous oil: 1H NMR (500 MHz, CDCl3) δ 1.08 (d, 3H), 1.37 (m, 2H), 1.48-1.68 (m, 6H), 2.55 (m, 4H), 2.74 (br, 2H), 2.92 (m, 1H), 3.18 (m, 2H), 3.58 (m, 1H), 3.72 (m, 1H), 4.70 (m, 1H), 4.80 (br, 1H), 5.08 (m, 4H), 6.92 (m, 1H), 7.08 (m, 5H), 7.22 (t, 1H), 7.34 (m, 10H), 7.92 (s, 1H), 8.31 (s, 1H); m/z (ESI) 638 [C39H47N3O5+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163758B2
Source datasetuspto-grants-2012_04
ORD IDord-01a5b76369b14de5a7354e365f319a1a
Source noteuspto-grants-2012_04