HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974849Generated: October 30, 2026
Water → (-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediol
https://huagongshe.com/reaction/1974849
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Dimethyl 2-(2-amino-6-chloropurin-9-ylmethyl)succinate | HCID 19027590 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | (-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediol | HCID 19027588 | 100% |
Reaction Steps
To a solution of (-)-dimethyl-2-(2-amino-6-chloropurin-9-ylmethyl)succinate (enantiomeric excess 85%; 19.9 mg, 0.0607 mmol), dissolved in tert. butanol (2.0 ml) at 40° C., was added lithiumborohydride (30 mg, 1.38 mmol) in portions with stirring. After 1 hr at ambient temperature, water (0.3 ml) was added slowly and stirring continued over night. Inorganic salts were filtered, washed carefully with tert. butanol and the solution was evaporated to dryness. Preparative thin-layer chromatography (PSC-Fertigplatten, Merck) with chloroform+methanol (5+1) as mobile phase afforded 16.5 mg (theoretical yield) of (-)-2-(2-amino-6-chloropurin-9-ylmethyl)-1,4-butanediol. [α]D20 °-5.20°, [α]54620 -5.92° (c 0.625, ethanol). TLC on silica (chloroform+methanol 5+1): Rf 0.40, identical to that of the racemate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05284837 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-dc7908f9d0104644897b489e1dcc7873 |
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| Source note | uspto-grants-1994_02 |
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