Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Reactant | Zidovudine | HCID 35370 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | HCID 54362158 | HCID 54362158 | — |
Reaction Steps
A solution of 280 mg AZT, 310 mg N-(3-bromopropyl)-phthalimide (BPP) and 300 ul of sodium methoxide solution (4.4M NaOMe in MeOH) in 1 ml DMPU was heated at 70° C. for one hour, then 145 mg BPP and 300 ul NaOMe solution was added and the mixture heated for another hour at 70° C. Another 175 mg BPP was added and heating was continued for a total of 4hours at 70° C. The reaction mixture was diluted with 10 volumes deionized water, acidified with 200 ul HOAc and extracted into EtOAc. The organic phase was washed with 5% NaHCO3, deionized water, 0.1M HOAc and saturated NaCl, then concentrated and chromatographed by preparative TLC on silica gel-F 2000 um using the solvent system CHCl3 /MeOH/HOAc(96.7+3.3+0.33). The product (Rf =0.35) was eluted with MeOH. It was immunologically active in an AZT assay by FPIA.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051361 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-739552566fbd47cd972e7c2e4af004b1 |
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| Source note | uspto-grants-1991_09 |
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