HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174294Generated: October 31, 2026
Sodium Hydroxide → 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyrimidin-4,5,6-triamine
https://huagongshe.com/reaction/2174294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | MeOH ACN DCM | HCID 22226298 | — |
| Reactant | 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine | HCID 69094074 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyrimidin-4,5,6-triamine | HCID 69093315 | 89% |
Reaction Steps
To a solution of 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine (Intermediate-7, 0.38 mmol) in DMF (2.5 mL) was added sodium hydroxide solution (2N, 3 equiv) and sodium dithionite (5.5 equiv). The reaction was heated to 150° C. and stirred for 2 h. The reaction mixture was diluted with CH2Cl2 and filtered. The filtrate was conc. and purified using SiO2 chromatography and an appropriate gradient (CH3CN/MeOH/CH2Cl2) to afford 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyrimidin-4,5,6-triamine as a tan solid (89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061030B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8b70105de56d47d89f5b1eab2c61bffe |
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| Source note | uspto-grants-2015_06 |
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