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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544864Generated: October 30, 2026

4-(Methylthio)benzoyl chloride → 4-Chloro-3-(4-(methylthio)phenylmethyl)-1-(beta-D-gluco-pyranosyl)indole

https://huagongshe.com/reaction/544864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylthio)benzoyl chlorideHCID 74042—
Reactant4-Chloro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indoleHCID 67020379—
Product4-Chloro-3-(4-(methylthio)phenylmethyl)-1-(beta-D-gluco-pyranosyl)indoleHCID 67196105—

Reaction Steps

4-Chloro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole obtained in Example 1-(3) and 4-(methylthio)benzoyl chloride were treated in a manner similar to Example 3 to give the titled compound as a colorless powder. APCI-Mass m/Z 450/452 (M+H). 1H-NMR (DMSO-d6) δ 2.43 (s, 3H), 3.24 (td, J=9.0, 5.6 Hz, 1H), 3.39 (td, J=8.7, 5.2 Hz, 1H), 3.43-3.48 (m, 2H), 3.62-3.69 (m, 2H), 4.23 (s, 2H), 4.53 (t, J=5.4 Hz, 1H), 5.09 (d, J=5.1 Hz, 1H), 5.16 (d, J=5.0 Hz, 1H), 5.21 (d, J=5.6 Hz, 1H), 5.40 (d, J=9.1 Hz, 1H), 7.02 (d, J=7.5 Hz, 1H), 7.10 (t, J=7.9 Hz, 1H), 7.17 (s, 4H), 7.27 (s, 1H), 7.54 (d, J=8.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935674B2
Source datasetuspto-grants-2011_05
ORD IDord-1708b27a0a1e4548bfe5ee17ac08650f
Source noteuspto-grants-2011_05