HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2'-Deoxy-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}cytidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Deoxycytidine hydrochloride | HCID 107488 | — |
| Reactant | Fluorenylmethyl chloroformate | HCID 14261773 | — |
| Product | 2'-Deoxy-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}cytidine | HCID 14309996 | 97% |
Reaction Steps
In one embodiment, 5′-O-DMTR-N4-FMOC-2′-deoxycytidine was prepared according to the following protocol. 30 g (37.9 mmol) of 2′-deoxycytidine hydrochloride were silylated with trimethylchlorosilane (75 ml) in pyridine (160 ml), followed by treatment with fluorenylmethoxycarbonyl chloride (33 g, 128 mmol). After hydrolysis with H2O (300 ml) and extraction with AcOEt/H2O, the N4-FMOC-2′-deoxycytidine was obtained in a 97% yield (49.5 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07667033B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-de5df47c417f476d9a3330a366acd292 |
| Source note | uspto-grants-2010_02 |