HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 13912578, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 13912575 | HCID 13912575 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 13912578 | HCID 13912578 | 106.8% |
Reaction Steps
A solution of 0.80 g (0.0014 mole) of 1-(Butylsulfonyl)-1, 6-dihydro-2-[[(4-methoxyphenyl) methyl]thio]-4-methyl-6-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, ethyl ester, 0.52 ml (0.0057 mole) of trifluoroacetic acid and 0.21 g (0.0032 mole) of ethanethiol in 15 ml of dichloromethane was stirred at room temperature for 24 hours. The solvent was evaporated, and the residue was flash chromatographed using ethyl acetate/ hexane (1:4) to give an oil which solidified very slowly. Trituration with isopropyl ether gave 0.33 g of the title compound as a colorless solid, melting point 118°-120° C. Analysis Calc'd. for C18H23N3O6S2 : C, 48.96; H, 5.25; N, 9.51; S, 14.52. Found: C, 48.99; H, 5.42; N, 9.32; S, 14.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684656 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-0823753611834577b41a22c78ed917ba |
| Source note | uspto-grants-1987_08 |