HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268435Generated: October 29, 2026
Methanol → 2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetic acid
https://huagongshe.com/reaction/2268435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-{9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetonitrile | HCID 59975293 | — |
| Product | 2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetic acid | HCID 59975282 | — |
Reaction Steps
A stirred solution of 2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetonitrile (preparation 30) (1.5 g, 3 mmol) in methanol (30 ml) and an aqueous 1 molar solution of sodium hydroxide (10 ml) was heated at reflux for 24 hr. The methanol was then removed under reduced pressure and the residual liquid diluted with more water and washed twice with ethyl acetate. The aqueous phase was acidified to pH<7 with a 1 molar aqueous citrc acid solution and then extracted twice with ethyl acetate. The extracts were combined, washed with brine and dried with anhydrous magnesium sulfate. The residue, after removal of the solvent under reduced pressure, was dissolved into diethyl ether and the solvent removed again twice under reduced pressure to give the title compound (1.25 g) as a foam. MS: 518 (M−H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326359B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-b9b1e6382cc04cbda5ebf4e8cd93ee2d |
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| Source note | uspto-grants-2001_12 |
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