HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 59975284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | N-benzyl-N-(2-{9-[(2R,3R,4R,5R)-3,4-bis{[tert-butyl(dimethyl)silyl]oxy}-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}ethyl)amine | HCID 69534115 | — |
| Product | HCID 59975284 | HCID 59975284 | 61.9% |
Reaction Steps
The title compound was prepared by a similar method to example 38 using N-benzyl-N-(2-{9-[(2R,3R,4R,5R)-3,4-bis{[tert-butyl(dimethyl)silyl]oxy}-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}ethyl)amine (360 mg, 0.44 mmol) (preparation 39) and a 1 molar solution of tetrabutylammonium fluoride in tetrahydrofuran (0.92 ml, 0.92 mmol). The product was purified by column chromatography on silica gel eluting with a solvent gradient of dichloromethane:methanol (93:7) increasing in polarity to dichloromethane:methanol:ammonia (90:10:1) to give the title compound (162 mg) as a foam. MS: 596 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326359B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-504b97c0ee83433caf04d00d2608afc1 |
| Source note | uspto-grants-2001_12 |