HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl isocyanate → HCID 13768039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl isocyanate | HCID 12668338 | — |
| Reactant | HCID 13768101 | HCID 13768101 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13768039 | HCID 13768039 | 61.3% |
Reaction Steps
1.94 g of 2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine are dissolved in anhydrous acetone, and 0.73 g of methanesulfonyl isocyanate is added thereto at room temperature. After the mixture is stirred for 30 minutes, the mixture is concentrated under reduced pressure to remove solvent. The residue is collected by filtration, and washed with water and ether, successively. The crude product thus obtained is recrystallized from a mixture of acetone and ether. 1.56 g of N-methanesulfonyl-2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazollidine-3-carboxamide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689327 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-4309e47a359d4d8aa7980c2c2a42a140 |
| Source note | uspto-grants-1987_08 |