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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710424Generated: November 2, 2026

Nicotinic Acid → [((alpha-Nicotinoyloxyisobutoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetic Acid

https://huagongshe.com/reaction/1710424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-{[(alpha-Chloroisobutoxy)carbonyl]aminomethyl}-Cyclohexane Acetic AcidHCID 22642007—
SolventAcetoneHCID 180—
Product[((alpha-Nicotinoyloxyisobutoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetic AcidHCID 1195921114.5%

Reaction Steps

A mixture of (93) (268 mg, 0.88 mmol), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (158 μL, 1.01 mmol), and nicotinic acid (637 mg, 5.2 mmol) in acetone was stirred at room temperature for 48 h. After filtration, the filtrate was concentrated in vacuo and the resulting residue was purified by reverse phase preparative HPLC to afford 50 mg (14%) of the title compound. 1H NMR (CD3OD, 400 MHz): δ 1.07 (d, J=6.8 Hz, 3H), 1.09 (d, J=6.8 Hz, 3H), 1.32-1.58 (m, 10H), 2.19 (m, 1H), 2.26 (s, 2H), 3.23 (m, 2H), 6.78 (d, J=4.8 Hz, 1H), 7.58 (m, 1H), 8.39 (d, J=6.4 Hz, 1H), 8.76 (d, J=4.4 Hz, 1H), 9.10 (s, 1H). MS (ESI) m/z 393.42 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790708B2
Source datasetuspto-grants-2010_09
ORD IDord-59653c36a1f54fc4ab8923fca5948b93
Source noteuspto-grants-2010_09