HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41369Generated: October 25, 2026
6-Desamino 6-Chloro Etravirine → Etravirine
https://huagongshe.com/reaction/41369
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Desamino 6-Chloro Etravirine | HCID 11751416 | — |
| Reactant | Ammonia dioxane | HCID 66648793 | — |
| Solvent | Water | HCID 962 | — |
| Product | Etravirine | HCID 193962 | 40.5% |
Reaction Steps
4-[[5-bromo-4-(4-cyano-2,6-dimethylphenoxy)-6-chloro-2-pyrimidinyl]amino]benzonitrile (0.00250 mol) and NH3/1,4-dioxane 0.5M (0.015 mol) were heated in a pressure vessel at 150° C. for 4 days. The sample was allowed to sit at ambient conditions for 2 days. Water was added slowly to the mixture until a precipitate formed. The mixture was stirred for 2 hours and filtered. The solid was recrystallized from CH3CN to obtain 0.58 g (fraction 1). The filtrate was evaporated (fraction 2). Both fractions were combined and purified by column chromatography, eluting with CH2Cl2. The resulting residue of the desired fraction was recrystallized from CH3CN to yield 0.44 g of 4-[[4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]amino]benzonitrile (40.5%). The sample was dried at 80° C. for 16 hours at 0.2 mm Hg (comp. 46).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530655B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-a571e09baa8c4edfa080376dad7e16dc |
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| Source note | uspto-grants-2013_09 |
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