HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345434Generated: October 30, 2026
N-Methylsulfamoyl chloride → HCID 19992426, compound
https://huagongshe.com/reaction/345434
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylsulfamoyl chloride | HCID 11789235 | — |
| Reactant | HCID 19992424 | HCID 19992424 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19992426 | HCID 19992426 | 39.6% |
Reaction Steps
Methylsulphamoyl chloride (0.39 g) was added dropwise to a stirred solution of 4-[(4-aminophenoxy)methyl]-1-[4-pyridyl]-piperidine (see Preparation 4) (0.57 g) in pyridine (15 ml) and the mixture was stirred at room temperature for 6 hours. An additional 0.39 g of methylsulphamoyl chloride was then added and the mixture was stirred for a further 18 hours and then evaporated. The residue was partitioned between sodium bicarbonate solution and ethyl acetate. The organic layer was separated and the aqueous layer was extracted several times with ethyl acetate. The combined organic layers were washed with water, dried (Na2SO4) and evaporated. The solid residue was crystallised from ethanol to give the title compound, (0.30 g), m.p. 170.5°-172.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057528 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-4dcc3d9b79ea4841b42825ae199dd4ca |
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| Source note | uspto-grants-1991_10 |
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