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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260708Generated: October 31, 2026

Diisopropylethylamine → HCID 178496555, compound

https://huagongshe.com/reaction/1260708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantRacemic trans-(3-methoxy-cyclopentyl)-acetic acid methyl esterHCID 59598533—
ReactantHCID 178478591HCID 178478591—
ReactantHCID 178504318HCID 178504318—
SolventDichloromethaneHCID 6344—
ProductHCID 178496555HCID 17849655568%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470828B2
Source datasetuspto-grants-2013_06
ORD IDord-60bdb4b885c44507b3258f7a923d8004
Source noteuspto-grants-2013_06