HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165552Generated: October 28, 2026
Dimethylformamide → 2-Amino-9-(2,2-dimethyl-1,3-dioxan-5-ylmethoxy)-6-methoxypurine
https://huagongshe.com/reaction/1165552
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-9-hydroxy-6-methoxypurine | HCID 14523963 | — |
| Reactant | 2,2-Dimethyl-5-iodo-methyl-1,3-dioxan | HCID 19813634 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Amino-9-(2,2-dimethyl-1,3-dioxan-5-ylmethoxy)-6-methoxypurine | HCID 19813631 | 70% |
Reaction Steps
A mixture of 2-amino-9-hydroxy-6-methoxypurine (50 mg, 0.276 mmol), 2,2-dimethyl-5-iodo-methyl-1,3-dioxan (70.6 mg, 0.276 mmol), potassium carbonate (40.1 mg, 0.290 mmol) and dimethylformamide (1 ml) was stirred at 20° C. for 3 hours. The suspension was diluted with chloroform (2 ml), filtered and the filtrate evaporated to dryness. The residue was chromatographed on silica gel (eluted with chloroform-ethanol, 100:1) yielding the title compound (59.6 mg, 70%). IR: νmax (KBr) 3396, 1640, 1581, 1480, 1390 cm-1 ; 1H NMR: δH [(CD3)2SO] 1.32 (3H, s, CH3), 1.35 (3H, s, CH3), 2.00 (1H, m, CH), 3.77 (2H, dd, J=11.8, 6.1 Hz, 2×H(ax)), 3.96 (3H, s, OCH3), 3.99 (2 H, dd, J=11.8, 4.1 Hz, 2×H(eq)), 4.36 (2H, d, J=6.8 Hz, CH2ON), 6.60 (2H, br.s, D2O exchangeable, NH2), 8.14 (1H, s, H-8). Found: C, 50.67; H, 6.31; N, 22.00%; m/e 309.1425. C13H19N5O4 +0.2 EtOH requires: C, 50.53; H, 6.41; N, 21.99%; m/e 309.1434.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04910307 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-e79218d9a7fe4859a43de64eba934f3d |
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| Source note | uspto-grants-1990_03 |
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