HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 6-Methoxymethoxy-N-[2-(4-thiomorpholinyl)ethyl]-1,2-benzisoxazol-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thiomorpholine, 4-(2-chloroethyl)- | HCID 96140 | — |
| Reactant | 3-Amino-6-methoxymethoxy-1,2-benzisoxazole | HCID 11008795 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Methoxymethoxy-N-[2-(4-thiomorpholinyl)ethyl]-1,2-benzisoxazol-3-amine | HCID 15435138 | 30% |
Reaction Steps
To a solution of 3-amino-6-methoxymethoxy-1,2-benzisoxazole (4.0 g) in N,N-dimethylformamide (DMF) (50 ml) was added sodium hydride (0.74 g) under nitrogen. The reaction was stirred one hours at ambient temperature. A solution of 4-(2-chloroethyl)thiomorpholine (3.6 g) in DMF (25 ml) was added to the reaction and heated to 125° C. for three hours. TLC (5% MeOH/CH2Cl2) revealed the absence of starting material. The reaction was diluted with EtOAc (1 l), washed with brine (4×500 ml), dried (MgSO4), and concentrated in vacuo. Flash column chromatography (silica gel) eluting with 5% acetone/CH2Cl2 afforded the the product (2.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046203 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-cdd0f4c677fd45a8aa3175e5cb60f0b8 |
| Source note | uspto-grants-2000_04 |