HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260708Generated: October 31, 2026
Diisopropylethylamine → HCID 178496555, compound
https://huagongshe.com/reaction/1260708
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 178478591 | HCID 178478591 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178496555 | HCID 178496555 | 68% |
Reaction Steps
A mixture of racemic trans-(3-methoxy-cyclopentyl)-acetic acid methyl ester [WO 2009/019174] (41 mg, 0.24 mmol) and KOSiMe3 (51 mg, 0.40 mmol) in CH2Cl2 (1 ml) was stirred at room temperature over night. The solvent was evaporated and DMF (1 ml) was added followed by trans-4-[2-(4-thieno[2,3-c]pyridin-7-yl-piperazin-1-yl)-ethyl]-cyclohexylamine trihydrochloride (intermediate A; 90 mg, 0.20 mmol), DIPEA (103 mg, 0.80 mmol) and TBTU (83 mg, 0.26 mmol). After stirring 3 h at room temperature, sat. aq. NaHCO3 sol. was added and the product was extracted with CH2Cl2. The organic layer was dried (MgSO4), the solvent was evaporated and the crude product was purified by flash chromatography on silica gel (CH2Cl2/MeOH 95:5) to yield the title compound as a light red foam (65 mg, 68%), MS (ISP) m/z=485.4 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470828B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-60bdb4b885c44507b3258f7a923d8004 |
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| Source note | uspto-grants-2013_06 |
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