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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404259Generated: October 31, 2026

Triethylamine → HCID 66615864, compound

https://huagongshe.com/reaction/1404259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantMethyl 2-((1r,4r)-4-(4-(5-aminopyridin-2-yl)phenyl)cyclohexyl)acetateHCID 66615773—
SolventDichloromethaneHCID 6344—
ProductHCID 66615864HCID 66615864—

Reaction Steps

To a mixture of {4-[4-(5-amino-pyridin-2-yl)-phenyl]-cyclohexyl}-acetic acid methyl ester (100 mg, 0.3 mmol) in methylene chloride (10 ml) was added triethylamine (43 ul, 0.3 mmol) and trimethylacetyl chloride (40 ul, 0.3 mmol). After 15 hours at room temperature, the reaction was diluted with hexanes to afford a precipitate which was collected by filtration: 1H NMR (400 MHz, DMSO-d6) δ ppm 1.15 (dd, J=12.69, 1.71 Hz, 2 H) 1.26 (s, 10 H) 1.42-1.56 (m, 1 H)1.50 (d, J=9.85 Hz, 1 H) 1.82 (d, J=11.37 Hz, 5 H) 2.26 (d, J=6.69 Hz, 2 H) 3.61 (s, 3 H) 7.32 (d, J=8.34 Hz, 2H) 7.87 (d, J=8.72 Hz, 1 H) 7.95 (d, J=8.34 Hz, 2 H) 8.15 (dd, J=8.72, 2.53 Hz, 1 H) 8.88 (d, J=2.53 Hz, 1 H)9.53 (s, 1 H); (M+H)+ 409.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912208B2
Source datasetuspto-grants-2014_12
ORD IDord-b426c8f649334e45858d7b8e68bf4f04
Source noteuspto-grants-2014_12