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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(4-iodo-1H-pyrazol-1-yl)cyclohexanone | HCID 59541165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[4-(4-Iodo-pyrazol-1-yl)-cyclohexylamino]-ethanol | HCID 89924440 | 86.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216991B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-30c243d268bb4206b1f31fdf8cdcfc34 |
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| Source note | uspto-grants-2015_12 |
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