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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365262Generated: October 30, 2026

methyl 6-(methylthio)nicotinate → HCID 58368201, compound

https://huagongshe.com/reaction/2365262

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 6-(methylthio)nicotinateHCID 901959—
ReactantHCID 68622221HCID 68622221—
ReactantHCID 68626060HCID 68626060—
ProductHCID 58368201HCID 58368201—

Reaction Steps

The title compound was prepared employing the procedures described for the construction of 2-[(1S,2S)-2-hydroxycyclohexyl]-5-{[6-(methylthio)pyridine-3-yl]methyl}-1,2-dihydro-3H-benzo[e]isoindol-3-one in Example 10, substituting 5-bromo-8-[(1S,2S)-2-hydroxycyclohexyl]-8,9-dihydro-7H-pyrrolo[3,4-h]quinolin-7-one for 5-bromo-2-[(1S,2S)-2-hydroxycyclohexyl]-1,2-dihydro-3H-benzo[e]isoindol-3-one, and substituting methyl 6-(benzyloxy)pyridine-3-carboxylate for methyl 6-(methylthio)nicotinate. The resultant white solid gave a proton NMR spectra consistent with theory: 1H NMR (400 MHz, CDCl3) δ 9.00-8.98 (m, 1H), 8.43-8.41 (m, 1H), 8.06 (s, 1H), 7.80 (s, 1H), 7.54-7.51 (m, 1H), 7.45-7.42 (m, 2H), 7.38-7.28 (m, 4H), 6.70 (d, J=8.5 Hz, 1H), 5.33 (s, 2H), 5.30-4.87 (m, 2H), 4.38 (s, 2H), 4.23-4.17 (m, 1H), 3.79-3.73 (m, 1H), 2.22-2.19 (m, 1H), 2.01-1.98 (m, 1H), 1.86-1.83 (m, 2H), 1.73-1.63 (m, 1H), 1.54-1.31 (m, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697690B2
Source datasetuspto-grants-2014_04
ORD IDord-fa0f5973262a4090a3884ec8ac2885a1
Source noteuspto-grants-2014_04