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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505686Generated: October 27, 2026

Ethanolamine → 2-[4-(4-Iodo-pyrazol-1-yl)-cyclohexylamino]-ethanol

https://huagongshe.com/reaction/1505686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-iodo-1H-pyrazol-1-yl)cyclohexanoneHCID 59541165—
SolventEthanolHCID 702—
Product2-[4-(4-Iodo-pyrazol-1-yl)-cyclohexylamino]-ethanolHCID 8992444086.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-ethanol (0.30 mL; 4.96 mmol; 1.4 eq.) was added in one portion to a solution of 4-(4-Iodo-pyrazol-1-yl)-cyclohexanone (intermediate 20; 1.00 g; 3.45 mmol; 1.0 eq.) in EtOH. After 1 h the reaction solution was cooled to 0° C. and NaBH4 (290 mg; 7.67 mmol; 2.2 eq.) added portionwise over 1 min. After a further 1 h the reaction suspension was poured into 1 N NaOH solution and extracted with DCM. Combined organic phases were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification using a SCX-2 cartridge afforded the title compound as a white solid (1.00 g; 84%). 1H NMR (300 MHz, DMSO) δ 7.94 (s, 1H), 7.49 (s, 1H), 4.47 (brs, 1H), 4.12 (m, 1H), 3.45 (m, 2H), 2.60 (t, J=5.8 Hz, 2H), 2.41 (m, 1H), 2.95 (m, 4H), 1.72 (m, 2H), 1.13 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216991B2
Source datasetuspto-grants-2015_12
ORD IDord-30c243d268bb4206b1f31fdf8cdcfc34
Source noteuspto-grants-2015_12