HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247350Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 21271463, compound
https://huagongshe.com/reaction/247350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | HCID 14391508 | HCID 14391508 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21271463 | HCID 21271463 | — |
Reaction Steps
To a solution of 3.0 g (0.01 mole) of 7-chloro-2-(2-chloroethyl)-2,3-dihydro-4,8-dimethylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione in 20 ml of dimethylsulfoxide was added ~5 g of sodium carbonate and 1.40 g (0.0245 mole) of azetidine. The reaction mixture was stirred for 2 days at room temperature and 0.3 g (0.005 mole) of azetidine was added and stirring continued for 3 days. The reaction mixture was poured in 300 ml of water. The aqueous mixture was extracted with 2×100 ml of benzene. The combined benzene extracts were washed with 3×75 ml of water, dried over sodium sulfate, filtered, and concentrated by rotary evaporation at 50° C. The residue was treated with oxalic acid in isopropyl alcohol which gave 3.5 g (82%) of yellow analytically pure crystals, m.p. 162°-66° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04705853 |
|---|
| Source dataset | uspto-grants-1987_11 |
|---|
| ORD ID | ord-3a39049b712d4f4db52f3b21c1d354a7 |
|---|
| Source note | uspto-grants-1987_11 |
|---|