HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612664Generated: November 1, 2026
HCID 19090048, compound → HCID 19090078, compound
https://huagongshe.com/reaction/1612664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19090048 | HCID 19090048 | — |
| Reactant | HCID 19090098 | HCID 19090098 | — |
| Product | HCID 19090078 | HCID 19090078 | 80.5% |
Reaction Steps
To 1.74 gm of 9-aminofuro[3,4-b]quinolin-1(3 H)-one was added 3.20 gm of 4-aminobutyl-1-benzylpiperidine, and the mixture was heated in a sealed tube for 6 hours at 200° C. while stirring. After cooling, the reaction mixture was recrystallized from ethyl acetate to obtain 3.00 gm of 9-amino- 2-(4-(1-benzYIpiperidYl)butyl)-2,3-dihydropyrrolo[3,4-b]quinolin-1-one (Compound (I) with R1 =R3 =H, R2 =NH2, A=>N-(CH2)n -, Y=>C=O, m=1, and n=4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05190951 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-d6c0b0d26d7a48c487bf5096848ed084 |
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| Source note | uspto-grants-1993_03 |
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