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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445129Generated: October 31, 2026

Ammonia → HCID 178428444, compound

https://huagongshe.com/reaction/1445129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSulfuric AcidHCID 1118—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 67142088HCID 67142088—
SolventWaterHCID 962—
ProductHCID 178428444HCID 17842844454.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

The compound prepared in Example 847 was treated with a saturated sodium bicarbonate solution to obtain 7-(3,4-dihydro-1H-isoquinolin-2-yl)-1-(3-fluorobenzyl)-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-5-amine. Concentrated sulfuric acid (1 ml) and water (5 ml) were added to 7-(3,4-dihydro-1H-isoquinolin-2-yl)-1-(3-fluorobenzyl)-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-5-amine (50 mg, 0.13 mmol) and then sodium nitrite (43.1 mg, 0.63 mmol) was added thereto. The reaction mixture was stirred for 5 minutes at 100° C. under heating and then excess ammonia solution was added thereto. The reaction mixture was stirred for 2 minutes under heating at the same temperature and then filtered to discard insoluble matertals. A potassium hydroxide solution was added to the reaction mixture, which was then filtered to discard insoluble matertals. The reaction mixture was extracted with ethyl acetate. The organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure to give 28.4 mg of the titled compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662832B2
Source datasetuspto-grants-2010_02
ORD IDord-756047fd585b4ff2bb8c28a96f7bed72
Source noteuspto-grants-2010_02