HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031180Generated: October 31, 2026
1-Methylpiperazine → HCID 86745733, compound
https://huagongshe.com/reaction/1031180
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-(2-Chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-one | HCID 19819759 | — |
| Reactant | Fumaric acid isopropyl alcohol | HCID 86745734 | — |
| Product | HCID 86745733 | HCID 86745733 | — |
Reaction Steps
To 20 mL of N-methylpiperazine was added 3.0 g (0.01 mol) of 2-(2-chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-one. The reaction mixture was heated to 60° C. for 24 hr. The excess amine was removed at 70° C., 0.5 mm Hg. The residual oil was taken up in 60 mL of CH2Cl2 and washed with 2×50 mL of 1N NaOH. The organic layer was dried over Na2SO4, filtered, concentrated by rotary evaporation, and further concentrated at 90° C., 0.5 mm Hg. The residual oil/glass was treated with 2 equivalent of fumaric acid isopropyl alcohol to give 3.4 g of solid. This was recrystallized from isopropyl alcohol to give 3.0 g (51%) off-white analytically pure material, mp 171°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05109013 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-8d2efe37b54f41a68976cb4e18bc5e84 |
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| Source note | uspto-grants-1992_04 |
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