HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377299Generated: October 31, 2026
1-Methylpiperazine → HCID 69202712, compound
https://huagongshe.com/reaction/2377299
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 69203023 | HCID 69203023 | — |
| Solvent | dichloromethane N,N-dimethylacetamide | HCID 85741463 | — |
| Product | HCID 69202712 | HCID 69202712 | — |
Reaction Steps
A mixture of Example 1094D (68 mg, 0.16 mmol), N-cyclohexylcarbodiimide-N′-methyl polystyrene (1.0 g, 1.28 mmol) and 1-hydroxybenzotriazole hydrate (44 mg, 0.33 mmol) in (2:1) dichloromethane/N,N-dimethylacetamide (10 mL) was agitated for about 15 min. 1-Methylpiperazine (77 mg, 0.77 mmol) was added, the mixture was agitated at room temperature for about 18 h, filtered and concentrated under vacuum. The residue was purified by flash column chromatography on silica gel using dichloromethane/methanol/ammonium hydroxide (100:8:0.1) as the mobile phase to provide the title compound. 1H NMR (500 MHz, DMSO-d6): δ 2.23 (s, 3H), 2.39 (m, 4H), 3.40 (m, 2H), 3.63 (m, 2H), 3.97 (s, 2H), 5.09 (s, 2H), 7.03 (m, 3H), 7.38 (m, 2H), 7.80 (s, 1H), 8.01 (m, 2H), 8.41 (s, 1H), 13.41 (s, 1H).MS (ESI): m/z 496 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468371B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-c5a217b6fd0d4bbd843291f3e89cacea |
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| Source note | uspto-grants-2008_12 |
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