HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 69539402, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | HCID 69539405 | HCID 69539405 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69539402 | HCID 69539402 | 80.9% |
Reaction Steps
To 3.0 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxyuridine was added 30 mL of chloroform, 0.72 g of triethylamine, 0.80 g (1.2 times moles of uridine derivative) of 1,4-diazabicyclo[2.2.2]octane and 1.36g of p-toluenesulfonyl chloride, and the resulting mixture was stirred at room temperature for 30 minutes. Ammonia gas was bubbled into the reaction mixture at room temperature for 1 hour, and the mixture was stirred in an ice bath for 1 hour. After sludging by the addition of 100 mL of water and 100 mL of methanol, the crystals were filtered and washed with the mixed solution of water and methanol (1:1) to give 2.42 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxycytidine. Yield 80.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822090B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-8bb5f2d8a5be4b48be30e40e256b24e2 |
| Source note | uspto-grants-2004_11 |