HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930507Generated: October 26, 2026
Isopropanol → 2-(pyridin-3-ylcarbonyl)-N-3-thienyl-1,2,3,4-tetrahydroisoquinolin-6-amine
https://huagongshe.com/reaction/930507
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Thiophen-3-amine | HCID 640543 | — |
| Reactant | (2-Chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanone | HCID 118970896 | — |
| Product | 2-(pyridin-3-ylcarbonyl)-N-3-thienyl-1,2,3,4-tetrahydroisoquinolin-6-amine | HCID 118970907 | 39.1% |
Reaction Steps
A solution of (2-chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanone, Intermediate 5 (0.025 g, 0.091 mmol) in isopropanol (0.1 mL) was treated with thiophen-3-amine (0.0099 g, 0.100 mmol). The resulting mixture was heated to 60° C. and allowed to stir overnight. After being allowed to cool to room temperature EtOAc (10 mL) was added to the reaction mixture, and the resulting solution was then washed twice with brine (10 mL). The combined aqueous layers were washed once with EtOAc (10 mL). The organic layers were combined, then dried over anhydrous Na2SO4(s), filtered and concentrated in vacuo. The resulting crude residue was then purified over silica using a MeOH/CHCl3 gradient. The desired product was obtained in 39.1% yield (0.012 g, 0.035 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296747B1 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-3ad152f8abcf4bc2967373e4ba6f2086 |
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| Source note | uspto-grants-2016_03 |
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