HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099148Generated: October 25, 2026
Triethylamine → N-[3-amino-2-methoxy-5-(1-methyl-cyclopropyl)-phenyl]-methanesulfonamide
https://huagongshe.com/reaction/2099148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Methoxy-5-(1-methyl-cyclopropyl)-benzene-1,3-diamine | HCID 17973087 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[3-amino-2-methoxy-5-(1-methyl-cyclopropyl)-phenyl]-methanesulfonamide | HCID 22025264 | 51% |
Reaction Steps
Triethylamine (521 μL, 3.74 mmol) was added to a solution of 2-methoxy-5-(1-methyl-cyclopropyl)-benzene-1,3-diamine (718 mg, 3.74 mmol) in methylene chloride at −10° C. Methanesulfonyl chloride (290 μL, 3.74 mmol) was then added dropwise over a 10 min period and the resultant solution was allowed to slowly warm to rt over 2 h. The mixture was quenched with saturated aqueous NaHCO3 and the aqueous layer was extracted with methylene chloride. The combined organic layers were dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (1% ammonium hydroxide/35% ethyl acetate in hexanes to 1% ammonium hydroxide/50% ethyl acetate in hexanes) provided a red solid which was triturated with a diethyl ether/hexanes (1:1) to yield Compound 1 (510 mg, 51%) as a pale brown solid: mp 144-146° C. ESI MS (m/z 271, M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569568B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-a9e59ae5231b4eb1b678169a09619b6a |
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| Source note | uspto-grants-2009_08 |
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