HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910641Generated: October 30, 2026
Diisopropylethylamine → HCID 58707252, compound
https://huagongshe.com/reaction/1910641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | HCID 58707332 | HCID 58707332 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58707252 | HCID 58707252 | 23% |
Reaction Steps
A mixture of N-(3,5-dichlorobenzyl)-5-fluoro-2-(methylsulfonyl)benzenamine (2.1 mmol), t-butyl piperazine-1-carboxylate (2.2 mmol), N,N-diisopropylethylamine (4.4 mmol) and acetonitrile (10 mL) was heated at reflux for 18 h, cooled to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate; this solution was washed with water, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using 10% ethyl acetate in hexanes as eluent to yield the title compounds as a yellow solid (23%). 1H NMR (400 MHz, CDCl3): δ 9.38 (br, 1 H), 7.67 (d, 1 H), 7.31 (s, 1 H), 7.21 (s, 2 H), 6.13 (dd, 1 H), 5.70 (d, 1 H), 4.42 (d, 2H), 3.54 (m, 4 H), 3.38 (m, 4 H), 1.49 (s, 9 H). MS (ESI) m/z: Calculated: 514.47; Observed: 515.6 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08604021B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-73a2a53f97e847eeb79dca2ca2f5ded0 |
|---|
| Source note | uspto-grants-2013_12 |
|---|