HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166706Generated: October 25, 2026
Dimethylformamide → (R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanine
https://huagongshe.com/reaction/1166706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine | HCID 136343267 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanine | HCID 135423395 | 45.7% |
Reaction Steps
A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mmol) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613936B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-ce81f07cfd82409393aacfb14c15ee65 |
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| Source note | uspto-grants-2003_09 |
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