HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052281Generated: October 28, 2026
Hydrochloric Acid → HCID 136005323, compound
https://huagongshe.com/reaction/2052281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | [1,2,4]Triazolo[4,3-a]quinazoline, 7-chloro-1-methyl-5-phenyl- | HCID 1869146 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136005323 | HCID 136005323 | 57.3% |
Reaction Steps
To a suspension of 1.3 g of 7-chloro-1-methyl-5-phenyl-s-triazolo[4,3-a]quinazoline in 70 ml of dimethylformamide was added 0.5 g of sodium borohydride. The mixture was heated with stirring at 75°-80° C. for 2 hours and then poured into ice-water. The resulting mixture was neutralized with dilute hydrochloric acid, and the precipitate formed was collected by filtration and washed with water. The solid was then suspended in a mixture of 40 ml of methanol and 5 ml of concentrated hydrochloric acid, and the mixture was stirred at room temperature for 2 hours. After neutralization with ammonia water, the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was recrystallized from dimethylformamideethanol to give 0.75 g of 7-chloro-4,5-dihydro-1-methyl-5-phenyl-s-triazolo[4,3-a]quinazoline as colorless needles, m.p. 262°-265° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04183932 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-7d1b58d5e5dd49e9b91ac0b77b7c893f |
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| Source note | uspto-grants-1980_01 |
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