HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 178478952, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | HCID 13588146 | HCID 13588146 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178478952 | HCID 178478952 | 29% |
Reaction Steps
A mixture of 7 parts of 6-chloro-N4 -[2-[4-[[-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]-4,5-pyrimidinediamine, 2.1 parts of carbon disulfide and 90 parts of N,N-dimethylformamide was stirred overnight at 70° c. The reaction mixture was poured into water. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from ethanol. The product was filtered off and dried in vacuo overnight at 120° C., yielding 2.3 parts (29%) of 7-[[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]amino]-thiazolo[5,4-d]pyrimidine-2-thiol monohydrochloride; mp. 226.5° C. (compound 148).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05126339 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-d11ea46af58a4931b1a13f7d1395e046 |
| Source note | uspto-grants-1992_06 |