HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553504Generated: November 1, 2026
Benzenesulfonyl chloride → HCID 67366550, compound
https://huagongshe.com/reaction/553504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 67367685 | HCID 67367685 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67366550 | HCID 67366550 | 75% |
Reaction Steps
Dissolve 2-[3′-(4-fluorophenyl)-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-yl]-ethylamine (0.099 g, 0.329 mmol) in dichloromethane (3 mL). Add resin-bound morpholine (0.145 g, 0.362 mmol) and shake at ambient temperature for 10 min. Add benzenesulfonyl chloride (0.064 g, 0.362 mmol)) and shake reaction at room temperature for 18 hr. Filter, concentrate and purify (SCX chromatography, followed by silica gel chromatography, eluting with 0:100 to 10:90 methanol:dichloromethane), to give free base of the title compound (109 mg, 75%). Dissolve the free base of the title compound (0.105 g, 0.238 mmol) in methanol and add a solution of ammonium chloride (0.013 g, 0.238 mmol) in a minimal volume of MeOH. Shake for 18 hr. at ambient temperature and concentrate to give the title compound (114 mg, 100%). MS (ES): m/z=442 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048884B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-7349c5b97a444708ae1761eaab902260 |
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| Source note | uspto-grants-2011_11 |
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