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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364920Generated: November 1, 2026

Pyridine → HCID 67116970, compound

https://huagongshe.com/reaction/2364920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantHCID 67117307HCID 67117307—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
ProductHCID 67116970HCID 6711697046.7%

Reaction Steps

Compound (2a) (340 mg, 1.05 mmol) was azeotroped three times with anhydrous pyridine. The mixture was added with anhydrous pyridine (2.0 ml) and 4,4′-dimethoxytrityl chloride (427 mg, 1.26 mmol) which has been deaerated for 1 hour, and subsequently with DMAP (38 mg, 0.31 mmol). Finally, triethylamine (170 μl, 1.26 mmol) was added and the mixture was stirred for 13 hours at room temperature. After characterization by TLC (CHCl3:MeOH=95:5), the product was purified with silica gel column chromatography using the development solvent of CHCl3 and MeOH while varying the ratio of CHCl3:MeOH from 98:2 to 95:5 to obtain the target Compound (3a) as a pale yellow solid (304 mg, 0.49 mmol, yield 46%). The target compound was determined by 1H NMR for identification. Further, mass analysis was carried out by MALDI-TOF MS and it was identified as the target compound (calcd. for C37H43N2O7 [M+H]+ 627.306, found 627.455).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697357B2
Source datasetuspto-grants-2014_04
ORD IDord-7de14aa621314eeca424394a69766dcb
Source noteuspto-grants-2014_04