HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511588Generated: October 26, 2026
Sodium cyanoborohydride → HCID 178501323, compound
https://huagongshe.com/reaction/511588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 5'-Amino-5'-deoxy-2',3'-O-(1-methylethylidene)-adenosine | HCID 11301215 | — |
| Reactant | Methyl 3-oxocyclobutane-1-carboxylate | HCID 13992367 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178501323 | HCID 178501323 | 41.2% |
Reaction Steps
A solution of methyl 3-oxocyclobutanecarboxylate (4.60 g, 35.94 mmol), 9-((3aR,4R,6R,6aR)-6-(aminomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine (11.0 g, 35.94 mmol) and Ti(iPrO)4 (4.0 g, 14.08 mmol) in MeOH (80 mL) was stirred at 45° C. for 2 h, then NaCNBH3 (4.5 g, 71.87 mmol) was added. The reaction was stirred at RT overnight. The reaction was quenched with aq. sat. NaHCO3 (40 mL) and filtered, extracted with DCM (80 mL×3), dried over Na2SO4 and concentrated. The residue was purified by preparative-HPLC to obtain the title compound (6.2 g, Yield 41%). 1H NMR (500 MHz, CDCl3): δH 8.38-8.34 (m, 1H), 7.90 (s, 1H), 5.98 (d, J=3.0 Hz, 1H), 5.75 (br s, 2H), 5.48-5.46 (m, 1H), 5.03-5.01 (m, 1H), 4.35-4.33 (m, 1H), 3.69-3.66 (m, 3H), 3.50-3.17 (m, 1H), 3.05-2.73 (m, 3H), 2.48-2.44 (m, 2H), 1.95-1.91 (m, 2H), 1.62 (s, 3H), 1.39 (s, 3H) ppm; ESI-MS (m/z): 419.2[M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096634B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-69c83961200d4f1d93b4e4fef1c240a3 |
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| Source note | uspto-grants-2015_08 |
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