HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → Phenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 5-Amino-1-methyl-4-phenoxycarbonylaminopyrazole | HCID 21904460 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamate | HCID 21904567 | 80.7% |
Reaction Steps
To a suspension of 5-amino-1-methyl-4-phenoxycarbonylaminopyrazole (153.8 g) in tetrahydrofuran (1 L) were added triethylamine (67 g) and triphenylmethyl chloride (185 g) at room temperature. The mixture was stirred for 6.5 hours. To the reaction mixture was added heptane (2.6 L) and the mixture was stirred for 1 hour. The precipitated solid was collected by filtration and washed with heptane-diisopropyl ether (1:1). The crude solid was suspended in water (3 L) and the suspension was stirred for 1 hour. The solid was collected by filtration and dried to give 1-methyl-4-phenoxycarbonylamino-5-triphenylmethylaminopyrazole (253.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192943B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-357565b0423249bda79dfe4b191372f4 |
| Source note | uspto-grants-2007_03 |