HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720636Generated: October 30, 2026
Hydrochloric Acid → 1-trityl-1H-[1,2,4]triazole-3-carboxylic acid {4-[3-butyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-amide
https://huagongshe.com/reaction/720636
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-trityl-1H-[1,2,4]triazole-3-carboxylic acid (4-{[6-amino-1-butyl-3-(2-fluoro-benzyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-ylcarbamoyl]-methyl}-phenyl)-amide | HCID 58739226 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-trityl-1H-[1,2,4]triazole-3-carboxylic acid {4-[3-butyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-amide | HCID 58739225 | 60.5% |
Reaction Steps
A solution of 1-trityl-1H-[1,2,4]triazole-3-carboxylic acid (4-{[6-amino-1-butyl-3-(2-fluoro-benzyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-ylcarbamoyl]-methyl}-phenyl)-amide (70 mg, 0.09 mmol) in methanol (3.0 mL) heated to 50° C. was treated with a 10% aqueous sodium hydroxide solution (1.08 mL). The reaction was heated at 50° C. for 4 h. At this time, the reaction was treated with a 3N aqueous hydrochloric acid solution (0.9 mL). This solution was stirred at 25° C. for 30 min. The resulting solids were collected by filtration, washed with water, and dried in vacuo to afford 1-trityl-1H-[1,2,4]triazole-3-carboxylic acid {4-[3-butyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-amide (41.3 mg, 60.5%) as a pale yellow solid: EI-HRMS m/e calcd for C45H39N8O3F (M+Na)+781.3027, found 781.3039.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135475B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-f70597494cc340ad95f7771c8ba75647 |
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| Source note | uspto-grants-2006_11 |
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