HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → HCID 20261265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester | HCID 157296 | — |
| Reactant | 4-(Difluoromethoxy)-6-methylpyrimidin-2-amine | HCID 2817390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20261265 | HCID 20261265 | 50% |
Reaction Steps
A solution of 6.2 g of 2-methoxycarbonyl-3-thienylsulfonylisocyanate in 50 ml of absolute tetrahydrofuran is stirred dropwise into a solution of 4.4 g of 2-amino-4-difluoromethoxy-6-methylpyrimidine in 80 ml of absolute tetrahydrofuran. During the course of this addition, the temperature of the reaction mixture rises from 20° to 26° C. After it has been stirred for another hour, the raction mixture is filtered and the filtrate is concentrated. The residue is crystallised from ethyl acetate, affording 5.3 g (50%) of N-(2-methoxycarbonyl-3-thienylsulfonyl)-N'-(4-difluoromethoxy-6-methylpyrimidin-2-yl)urea (compound 2.1) with a melting point of 178°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04549898 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-3086ea1c378a4a7e855846d0a83f48ec |
| Source note | uspto-grants-1985_10 |