HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416746Generated: October 30, 2026
Diisopropylethylamine → HCID 57897211, compound
https://huagongshe.com/reaction/416746
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(4-fluorobenzyl)-1,4-diazepane | HCID 2774433 | — |
| Reactant | 5-Bromo-4-chloro-3-nitropyridin-2-amine | HCID 45480236 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 57897211 | HCID 57897211 | — |
Reaction Steps
To a mixture of 5-bromo-4-chloro-3-nitro-pyridin-2-ylamine (0.126 g, 0.50 mmol) and isopropanol (9 ml) was added 1-(4-fluorobenzyl)-1,4-diazepane×2HCl (0.155 g, 0.55 mmol) followed by diisopropylethylamine (0.30 ml, 1.70 mmol). The reaction mixture was heated at 45° C. for 24 h, then allowed to cool to room temperature. The precipitate was collected by filtration and washed with isopropanol and diethyl ether. The title compound was thus obtained as a yellow solid (0.110 g, 52%); 1H-NMR (500 MHz, DMSO-d6) 1.82 (m, 2H), 2.67 (m, 4H), 3.17 (m, 2H) and 3.24 (t, J=5.85 Hz, 2H) (homopiperazine protons), 3.61 (s, 2H, N—CH2), 6.95 (s, 2H, NH2), 7.15 (t, J=9.10 Hz, 2H) and 7.35 (dd, J=10.20, 3.60 Hz, 2H) (3,5-ArH and 2,6-ArH), 8.17 (s, 1H, 6-H);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088761B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-96eedca044134d3a85e384a2ebd72e7d |
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| Source note | uspto-grants-2012_01 |
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