Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704306Generated: October 30, 2026

1H-Pyrrolo[2,3-b]pyridine, 2,3-dihydro-1,3,3-trimethyl-2-methylene- → HCID 15100094, compound

https://huagongshe.com/reaction/704306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo[2,3-b]pyridine, 2,3-dihydro-1,3,3-trimethyl-2-methylene-HCID 170513—
Reactant3,5-Dimethoxy-2-nitrosophenolHCID 14419270—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 15100094HCID 15100094—

Reaction Steps

Into a three-necked 100 milliliter round bottom flask was charged a solution of 0.8 grams of the thus prepared 1,3,3-trimethyl-2-methylene-1,7-diazaindane in 20 milliliters of absolute ethanol. The solution was heated under a nitrogen pad to 60°-65° C. and 0.84 grams of 2-nitroso-3,5-dimethoxyphenol added to the flask. The reaction mixture was maintained at temperature and refluxing for a total reaction time of about 26 hours. The ethanol was removed on a rotary evaporator and the resulting reaction mixture taken up in ether and filtered. The ether solution sequentially was washed with 100 milliliters of a 10 percent sodium hydroxide solution, and 100 milliliters of a saturated sodium chloride solution and then dried over potassium carbonate. The ether was removed under vacuum. A silica gel column was used to isolate the final product, i.e., 1',3'-Dihydro-1',3',3'-trimethyl-5,7-dimethoxyspiro-[2H-1,4-benzoxazine-2,2'-[2H] pyrrolo[2,3-b]pyridine]. Identification of the product was confirmed by appropriate spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04986934
Source datasetuspto-grants-1991_01
ORD IDord-e0bc184219814d06869d48ae1b1454a8
Source noteuspto-grants-1991_01