HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262988Generated: November 2, 2026
Sodium Hydroxide → 2-chloro-4-(o-chlorophenyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine-9-methanol
https://huagongshe.com/reaction/262988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-chloro-4-(o-chlorophenyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine-9-carboxylic acid ethyl ester | HCID 70600872 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-chloro-4-(o-chlorophenyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine-9-methanol | HCID 21317687 | — |
Reaction Steps
A solution of 0.41 g of 2-chloro-4-(o-chlorophenyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine-9-carboxylic acid ethyl ester in 6.5 ml of absolute tetrahydrofuran is added dropwise with ice-cooling and stirring to a suspension of (0.078 g) of lithium aluminium hydride in 5 ml of absolute tetrahydrofuran. After stirring for 1 hour at 5° C., there is added dropwise 0.8 ml of 0.5-N sodium hydroxide. After filtration of the solid material, the solvent is evaporated and the residue taken up in methylene chloride. The solution is washed with 0.5-N sodium hydroxide, subsequently with water and, after drying, evaporated to dryness. By crystallization of the residue from ethyl acetate, there is obtained 2-chloro-4-(o-chlorophenyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine-9-methanol, melting point 219°-221° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04155913 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-dd7103d1969d4caab51b0fba7ac39deb |
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| Source note | uspto-grants-1979_05 |
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