HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 4-(1-(naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxy-2,6-dimethylbenzene-1-sulfonyl chloride | HCID 15917496 | — |
| Reactant | Methyl 4-(piperidin-2-yl)butanoate hydrochloride | HCID 66772062 | — |
| Product | Methyl 4-(1-(naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoate | HCID 57904267 | 79% |
Reaction Steps
The sulfonyl chloride 1 (9.76 g, 85.2 mmol) and Et3N (11.8 ml, 85.2 mmol) were dissolved in CH2Cl2 (100 ml), and a solution of diphenylmethanamine (2, 15.61 g, 85.2 mmol) in CH2Cl2 (40 ml) was added dropwise in the course of 10 min. The reaction mixture was stirred at room temperature for 18 h. The reaction mixture was washed with aqueous 0.5 M KHSO4 (2×200 ml) and sat. NaCl solution (100 ml), dried over Na2SO4 and concentrated to dryness. Recrystallization from CH2Cl2 at 0-5° C. gave 17.63 g (79%) of the sulfonamide 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318769B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-cf7f4129a0f24a0b98daca5c89f6ae79 |
| Source note | uspto-grants-2012_11 |