HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16899Generated: October 30, 2026
1-(Prop-2-en-1-yl)-1,4-diazepane → HCID 178456266, compound
https://huagongshe.com/reaction/16899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Prop-2-en-1-yl)-1,4-diazepane | HCID 22921984 | — |
| Reactant | HCID 178489782 | HCID 178489782 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178456266 | HCID 178456266 | 69% |
Reaction Steps
1-Prop-2-enyl-1,4-diazepane (224 mg, 1.60 mmol) was added to 5-chloro-N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]pyrazine-2-carboxamide (310 mg, 0.80 mmol) in DMSO (4.00 ml) at 25° C. The resulting solution was stirred at room temperature for 3 h. The reaction mixture was diluted with MeOH (5 ml) and the crude product was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford crude product as an orange oil. The crude product was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (271 mg, 69%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737149B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d8f52469cd624662af37e192f5b37d03 |
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| Source note | uspto-grants-2010_06 |
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