HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 10,11-dihydro-5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine | HCID 14601947 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 10,11-dihydro-5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine | HCID 14601948 | 74% |
Reaction Steps
A solution of 4.2 g of 5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine in 75 ml of ethanol, was treated with 800 mg of sodium borohydride and stirred at ambient temperature for 18 hours. The solvent was then concentrated in vacuo and the residue taken up in water and extracted with ethyl acetate (2×). The combined organics were washed with water followed by a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated. The resultant solid was recrystallized from isopropyl ether:methanol (180:10) to afford 3.1 g (74%) of 10,11-dihydro-5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine, m.p. 135°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996205 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-3df724ceaf5a4933acbb4cf28e71da24 |
| Source note | uspto-grants-1991_02 |