HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483143Generated: November 2, 2026
Methanesulfonyl chloride → HCID 131714589, compound
https://huagongshe.com/reaction/483143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(3-Aminophenyl)-1,4-dihydroisoquinol-3-one | HCID 20242553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 131714589 | HCID 131714589 | 48.7% |
Reaction Steps
A solution of 1-(3-aminophenyl)-1,4-dihydroisoquinol-3-one (8.0 g) in dichloromethane (500 ml) and triethylamine (50 ml) was treated dropwise, at room temperature, with a solution of mesyl chloride (9.7 g) in dichloromethane (20 ml). After stirring for 3 h, the resulting precipitate (m.p. 251°-253° C.) was collected, washed with dichloromethane, water, and air dried. The product was stirred with a mixture of 10% aqueous sodium hydroxide (200 ml) and methanol (20 ml) at 50° C. for 1 h. The mixture was filtered and the filtrate was evaporated to one third volume in vacuo. It was acidified with dilute hydrochloric acid, and the resulting precipitate was collected and washed with water. Recrystallisation from methanol-ether afforded the title compound (3.55 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578393 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-4794dafb8d5f4a8babe4dcf675b28e02 |
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| Source note | uspto-grants-1986_03 |
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