HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689947Generated: November 1, 2026
1,4-Dichlorophthalazine → (R)-tert-butyl 4-(4-chlorophthalazin-1-yl)-3-methylpiperazine-1-carboxylate
https://huagongshe.com/reaction/1689947
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dichlorophthalazine | HCID 78490 | — |
| Reactant | (R)-1-Boc-3-methylpiperazine | HCID 2756811 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-tert-butyl 4-(4-chlorophthalazin-1-yl)-3-methylpiperazine-1-carboxylate | HCID 57581470 | — |
Reaction Steps
1,4-dichlorophthalazine (5.00 g, 25.1 mmol) and (R)-tert-butyl 3-methylpiperazine-1-carboxylate (11.06 g, 55.2 mmol) were mixed intimately and placed in a flask under an Argon atmosphere. The flask was heated at 120° C. for approximately 16 hours, after which time LC/MS showed disappearance of the starting material. The reaction was cooled, taken up in dichloromethane (150 mL), and washed once with aqueous sodium bicarbonate (50% of saturated) and once with saturated sodium chloride solution. The organic phase was dried (MgSO4) and evaporated to give an orange oil. Chromatography over silica gel with a gradient of hexanes/0-10% acetone gave a pale yellow solid JK-1. MS (M+H)+=363.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153633B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-00ab3d46dd16498db60ee8f4c60e06c4 |
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| Source note | uspto-grants-2012_04 |
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