HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 1-cyclohexyl-3-{[3-[3,6-dihydro-1(2H)-pyridinecarbonyl]-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]sulfonyl}urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 1,2,3,6-Tetrahydropyridine | HCID 12750 | — |
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | 1,2,3,6-Tetrahydropyridine-1-carbonyl chloride | HCID 13094830 | — |
| Reactant | 2,3,4,5-tetrahydro-1H-3-benzazepine-7-sulfonamide hydrochloride | HCID 21434429 | — |
| Reactant | 3-[3,6-dihydro-1(2H)-pyridinecarbonyl]-2,3,4,5-tetrahydro-1H-3benzazepine-7-sulfonamide | HCID 21434438 | — |
| Product | 1-cyclohexyl-3-{[3-[3,6-dihydro-1(2H)-pyridinecarbonyl]-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]sulfonyl}urea | HCID 54210304 | — |
Reaction Steps
By the reaction of 3-[3,6-dihydro-1(2H)-pyridinecarbonyl]-2,3,4,5-tetrahydro-1H-3benzazepine-7-sulfonamide with cyclohexylisocyanate in a manner analogous to that described in Example 1, there is obtained 1-cyclohexyl-3-{[3-[3,6-dihydro-1(2H)-pyridinecarbonyl]-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-sulfony(} urea, m.p. 173°-174° C. The starting material can be prepared by first reacting 1,2,3,6-tetrahydropyridine with phosgene and subsequently bringing the resulting 3,6-dihydro-1(2H)-pyridinecarbonyl chloride to reaction with 2,3,4,5-tetrahydro-1H-3-benzazepine-7-sulfonamide hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024128 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-3049118b2e0942aa87ebfcdd9c00729b |
| Source note | uspto-grants-1977_05 |