HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 69539402, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Uridine | HCID 6029 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | HCID 69539405 | HCID 69539405 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69539402 | HCID 69539402 | 54% |
Reaction Steps
To 1.0 g of 3′,5′-O-bis (4-chlorobenzoyl)-2′-deoxyuridine was added 5 mL of acetonitrile, 0.40 g of triethylamine, 0.24 g (1.2 times moles based on the uridine derivative) of 1-methylpiperidine and 0.76 g of p-toluenesulfonyl chloride, and the reaction mixture was stirred in an ice bath for 2 hours. To this, 7.5 mL of a solution of ammonia in 2-propanol was added, and the mixture was stirred in an ice bath for 4 hours, and at room temperature for 1 hour. The crystals were filtered and washed with acetonitrile to give 0.54 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxycytidine. Yield 54%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822090B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-91b52cbdb84c47e4a2dd6c5bd92e10c2 |
| Source note | uspto-grants-2004_11 |