HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633306Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 22828235, compound
https://huagongshe.com/reaction/1633306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-(((Tert-butoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acid | HCID 4164897 | — |
| Reactant | HCID 54526695 | HCID 54526695 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22828235 | HCID 22828235 | 35.3% |
Reaction Steps
A mixture of methyl-1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-amino-β-D-ribofuranuronate (294 mg) prepared in Example 62, N-tert-butoxycarbonyl-β-(4-chlorophenyl)-D,L-alanine (300 mg) and N,N'-dicyclohexylcarbodiimide (206 mg) in tetrahydrofuran (15 ml) and water (5 ml) was stirred overnight. The mixture was diluted with water (50 ml) and extracted with ethyl acetate. The extract was washed with water, dried, and evaporated to dryness. The residue was subjected to column chromatography on silica gel. The elution was carried out with a mixed solvent (chloroform/methanol=97/3). The eluate was evaporated to dryness to give methyl 1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-[N-tert-butoxycarbonyl-β-(4-chlorophenyl)-D,L-alanylamino]-β-D-ribofuranuronate (203 mg), mp. 120°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04479942 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-16100e2a11cb4fbab579b8d51d43be9f |
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| Source note | uspto-grants-1984_10 |
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