HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042411Generated: November 3, 2026
Diisopropylethylamine → HCID 178496556, compound
https://huagongshe.com/reaction/2042411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | Racemic trans-(3-methoxy-cyclopentyl)-acetic acid methyl ester | HCID 59598533 | — |
| Reactant | HCID 178478592 | HCID 178478592 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178496556 | HCID 178496556 | 78.5% |
Reaction Steps
A mixture of racemic trans-(3-methoxy-cyclopentyl)-acetic acid methyl ester [WO 2009/019174] (70 mg, 0.41 mmol) and KOSiMe3 (88 mg, 0.69 mmol) in CH2Cl2 (1.5 ml) was stirred at room temperature over night. The solvent was evaporated and DMF (1.5 ml) was added followed by trans-4-[2-(4-furo[3,2-c]pyridin-4-yl-piperazin-1-yl)-ethyl]-cyclohexylamine trihydrochloride (intermediate A) (150 mg, 0.34 mmol), DIPEA (177 mg, 1.37 mmol) and TBTU (143 mg, 0.44 mmol). After stirring 4 h at room temperature, sat. aq. NaHCO3 sol. was added and the product was extracted with CH2Cl2. The organic layer was dried (Na2SO4), the solvent was evaporated and the crude product was purified by flash chromatography on silica gel (CH2Cl2/MeOH/25% NH3 aq 140:10:1) to yield the title compound as a white solid (125 mg, 78%), MS (ISP) m/z=469.3 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586579B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-55e76aa2526440e1b2b10e0f032d7df8 |
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| Source note | uspto-grants-2013_11 |
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