HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697862Generated: November 2, 2026
Methanesulfonyl chloride → HCID 58049436, compound
https://huagongshe.com/reaction/1697862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzyl (1-(hydroxymethyl)cyclopropyl)carbamate | HCID 22178711 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58049436 | HCID 58049436 | — |
Reaction Steps
N-CBZ-amino-1-(hydroxymethyl)cyclopropane (similarly prepared according to JMC 31, 2004, 1998) (250 mg) was dissolved into DCM (25 ml) with DIPEA (250 l) and stirred at 0° C. for 15 minutes. To the reaction was added MsCl (1.1 eq) and stirred for 30 minutes. The reaction was washed with NaHCO3 solution, water, brine and dried with Na2SO4. The solution was evaporated to give N-CBZ-amino-1-(methylsulfonyloxymethyl)cyclopropane as an off white solid. This solid was mixed with above 6-(7-hydroxy-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide and Cs2CO3 (250 mg) in DMA (4 ml). The reaction was heated at 100° C. for 10 hours and mixed with EtOAc and water, then filtered, further extracted with EtOAc. The combined organic layer was evaporated and purified with silica gel column to give the titled product. Mass: (M+1), 578
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163923B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-13e46f1cb61f4390b44b68ec50dd82ed |
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| Source note | uspto-grants-2012_04 |
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