HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804086Generated: October 31, 2026
4-Bromo-2-methylaniline → HCID 67380949, compound
https://huagongshe.com/reaction/1804086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-2-methylaniline | HCID 11423 | — |
| Reactant | N,N-bis(2-chloroethyl)-p-toluenesulphonamide | HCID 96039 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Product | HCID 67380949 | HCID 67380949 | 35.2% |
Reaction Steps
By reaction and treatment in the same manner as in Preparation Example 15 and using 4-bromo-2-methylaniline (3 g), N,N-bis(2-chloroethyl)-4-methylbenzenesulfonamide (5.65 g) and cyclopropylboronic acid (721 mg), 1-(4-cyclopropyl-2-methylphenyl)piperazine (640 mg) was obtained. To a solution (7 mL) of 6-bromonicotinic acid (132 mg) in methanol were added 1-(4-cyclopropyl-2-methylphenyl)piperazine (150 mg) and 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (DMT-MM) (217 mg), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (ethyl acetate:hexane) to give the title compound (260 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354401B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-55ff69408e3a46e0a701ee1e91161f0d |
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| Source note | uspto-grants-2013_01 |
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