HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878403Generated: October 31, 2026
Diisopropylethylamine → HCID 57917641, compound
https://huagongshe.com/reaction/1878403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 3-(chloromethyl)-4-methoxybenzoate | HCID 12853097 | — |
| Reactant | HCID 57917584 | HCID 57917584 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57917641 | HCID 57917641 | 43% |
Reaction Steps
1-Phenyl-3-(4-(piperazin-1-carbonyl)phenyl)urea (439 mg, 1.0 mmol) was stirred in acetonitrile (8 mL) at room temperature for 1 hour, N-Ethyl-N-isopropylpropan-2-amine (697 μl, 4 mmol) was added, followed by a solution of methyl 3-(chloromethyl)4-methoxy-benzoate (215 mg, 1.0 mmol) in acetonitrile (5 mL). The mixture was heated to 45° C. and stirred overnight. The mixture was concentrated under vacuum, diluted with dichloromethane (40 mL) and washed with saturated aqueous ammonium chloride (25 mL) and saturated aqueous sodium chloride (25 mL). The organic phase was dried on magnesium sulfate, filtered and concentrated under vacuum. The residue was submitted to silica chromatography (0-10% methanol in dichloromethane as eluant) to give the title compound (216 mg). MS (ESI) m/z 503.1 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314091B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c6675fb6d5e24748a5f5799a4898322a |
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| Source note | uspto-grants-2012_11 |
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