HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354063Generated: October 31, 2026
Diisopropylethylamine → HCID 11952786, compound
https://huagongshe.com/reaction/1354063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2,3-Dichlorophenyl)piperazine hydrochloride | HCID 11630372 | — |
| Reactant | HCID 22029304 | HCID 22029304 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 11952786 | HCID 11952786 | — |
Reaction Steps
A mixture of 1-(2,3-dichlorophenyl)piperazine hydrochloride (8.0 g) and diisopropylethylamine (15 mL) in butanone (50 mL) was heated to 45° C. followed by the addition of 5-bromo-1-(2,3-dihydro-1H-indol-1-yl)pentan-1-one (5.4 g). The resulting mixture was boiled under reflux for 40 h and filtered hot. The remaining organic phase was left to crystallise, and a white crystalline material was collected by filtration and washed with acetone (3.8 g). Mp 121–123° C. 1H NMR (DMSO-d6): 1.50–1.70 (m, 4H); 2.30–2.65 (m, 8H); 3.00 (s, 4H); 3.15 (t, 2H); 4.10 (t, 2H); 6.95 (t, 1H); 7.10–7–15 (m, 2H); 7.20 (d, 1H); 7.25–7.35 (m, 2H); 8.10 (d, 1H). MS m/z: 432 (MH+), 315, 202.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223765B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-2c79c8171908420d94e8a62ad64f3174 |
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| Source note | uspto-grants-2007_05 |
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