HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447129Generated: October 29, 2026
4-Methylmorpholine → HCID 59191578, compound
https://huagongshe.com/reaction/447129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | HCID 59191594 | HCID 59191594 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59191578 | HCID 59191578 | 81.6% |
Reaction Steps
To a solution of 3-benzyl-4,5-dimethyl-6-piperazin-1-yl-pyridazine (60 mg, 0.21 mmol) and phenyl chloroformate (40 mg, 0.26 mmol) in CH2Cl2 (3 mL) at 25° C. is added N-methyl morpholine (0.07 mL, 0.60 mmol). After being stirred at 25° C. for 3 h, the mixture is diluted with CH2Cl2 (10 mL), and washed with saturated sodium bicarbonate (1 mL) and water (2×5 mL). The organic layer is concentrated and purified by HPLC (CH3CN/H2O: 22%˜45% with 0.1% TFA) to give 4-(6-benzyl-4,5-dimethyl-pyridazin-3-yl)-piperazine-1-carboxylic acid phenyl ester (69 mg, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481542B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-d3da6da9e78c4c06997219e3e513b826 |
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| Source note | uspto-grants-2013_07 |
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