HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 21910602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 21910636 | HCID 21910636 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21910602 | HCID 21910602 | 34% |
Reaction Steps
4-Bromomethyl-3-(4-chlorophenyl)-2-thia-1-azaspiro[4.5]dec-3-ene 2,2-dioxide, made as described in Example 2, (270 mg, 0.69 mmol) was dissolved in ethanol (30 mL). Methylamine (70% solution in water, 8 mL) was added and the mixture was stirred overnight at room temperature and concentrated. The residue was dissolved in CH2Cl2, washed with water and extracted with 0.5 M HCl. After addition of NaOH and extraction with CH2Cl2 the organic layer was dried (Na2SO4) and evaporated to yield 80 mg (34%) of 3-(4-Chlorophenyl)-4-methylaminomethyl-2-thia-1-azaspiro[4.5]dec-3-ene 2,2-dioxide as a solid. MS (IS): 341 [MH]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125840B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-a6a46054166e47f188ff562b861fc636 |
| Source note | uspto-grants-2006_10 |