HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886145Generated: October 30, 2026
2-(Isopropylamino)ethanol → HCID 58204314, compound
https://huagongshe.com/reaction/886145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Isopropylamino)ethanol | HCID 7994 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86652301 | HCID 86652301 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 58204314 | HCID 58204314 | 68% |
Reaction Steps
Following the procedure for 116, 8-bromo-4,5-dihydro-6-oxa-1,10b-diaza-benzo[e]azulene-2-carboxylic acid was reacted with 2-isopropylamino-ethanol. The intermediate formed (145 mg, 0.37 mmol) was dissolved in IMS (10 mL) and triethylamine (50 μL, 0.37 mmol) then 10% Pd/C (20 mg) added before the reaction mixture stirred under hydrogen (1 atmosphere) for 2.75 h. The reaction mixture was filtered through Celite® and the filtrate concentrated in vacuo. The resultant residue was partitioned between DCM and water, the aqueous layer was isolated and extracted with DCM. The combined organic extracts dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was dissolved in diethyl ether and the solution washed with water, dried (Na2SO4), filtered and then concentrated in vacuo to give 140 (79 mg, 68%). 1H NMR (DMSO-d6, 400 MHz): δ 7.83 (dd, J=8.0, 1.6 Hz, 1H); 7.30 (td, J=7.6, 1.8 Hz, 1H); 7.26-7.16 (m, 2H); 6.54 (s, 1H); 4.67-4.53 (m, 1H); 4.46 (t, J=6.0 Hz, 2H); 4.35-4.27 (m, 1H); 3.64-3.56 (m, 2H); 3.55-3.46 (m, 2H); 3.13 (t, J=6.0 Hz, 2H); 1.22 (d, J=6.8 Hz, 6H). LCMS: RT=9.00 min, M+H+=316
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242104B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-3330a7e7ab2542daabe831a5eb04a3b8 |
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| Source note | uspto-grants-2012_08 |
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