HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215747Generated: October 25, 2026
Potassium Carbonate → 4-(4-Methyl-piperazin-1-yl)-6,7,8,9-tetrahydro-benzo[4,5]thieno[3,2-d]pyrimidin-2-ylamine
https://huagongshe.com/reaction/215747
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 4-Chloro-6,7,8,9-tetrahydrobenzo[4,5]thieno[3,2-D]pyrimidin-2-amine | HCID 57617680 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Methyl-piperazin-1-yl)-6,7,8,9-tetrahydro-benzo[4,5]thieno[3,2-d]pyrimidin-2-ylamine | HCID 25226775 | 44.5% |
Reaction Steps
To a solution of 4-chloro-6,7,8,9-tetrahydro-benzo[4,5]thieno[3,2-d]pyrimidin-2-ylamine (0.09 mg, 0.37 mmol) in EtOH (3.7 mL) was added K2CO3 (0.12 g, 0.84 mmol) followed by N-methylpiperazine (0.05 mL, 0.44 mmol). After stirring at rt for 22 h, EtOH was removed under reduced pressure and the mixture was dissolved in CH2Cl2 (5 mL) and poured over H2O (10 mL). The aqueous layer was extracted with CH2Cl2 (3×10 mL). The combined organic layers were washed with brine, such as with a satd. aq. NaCl, (30 mL), dried, for example with Na2SO4, and concentrated to afford the title compound (0.05 g) as a pale yellow solid. MS: 304.2. 1H NMR (400 MHz, CD3OD) δ ppm 3.93-3.88 (m, 4H), 2.80 (t, J=6.0 Hz, 2H), 2.63 (t, J=6.1 Hz, 2H), 2.56-2.52 (m, 4H), 2.33 (s, 3H), 1.96-1.81 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193178B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-cfb97103f1504555a405b664868daf5e |
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| Source note | uspto-grants-2012_06 |
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