HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiolan-3-amine → 3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-(tetrahydrothiophen-3-ylamino)-cyclobut-3-ene-1,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiolan-3-amine | HCID 522918 | — |
| Reactant | 3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-ethoxy-cyclobut-3-ene-1,2-dione | HCID 86641802 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-(tetrahydrothiophen-3-ylamino)-cyclobut-3-ene-1,2-dione | HCID 25112996 | — |
Reaction Steps
The title compound is prepared from 3-(4-chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-ethoxy-cyclobut-3-ene-1,2-dione analogously to 6-chloro-2-hydroxy-N,N-dimethyl-3-{2-[(R)-1-((2R,5R)-5-methyl-tetrahydrofuran-2-yl)-propylamino]-3,4-dioxo-cyclobut-1-enylamino}-benzenesulfonamide (Example 3) by replacing (R)-1-((2R,5R)-5-methyl-tetrahydrofuran-2-yl)-propylamine p-toluenesulfonate salt with tetrahydrothiophen-3-ylamine. The reaction is carried out in EtOH. The title compound is obtained. MH+ 403.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183281B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-f81461ffc2dc43ee85f7fd900d6c25cd |
| Source note | uspto-grants-2012_05 |