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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863693Generated: October 30, 2026

Triethylamine → HCID 19696422, compound

https://huagongshe.com/reaction/863693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonic anhydrideHCID 81560—
ReactantHCID 10130409HCID 10130409—
SolventDichloromethaneHCID 6344—
ProductHCID 19696422HCID 19696422—

Reaction Conditions

Temperature80 °C

Reaction Steps

2.4 g of methanesulfonic anhydride and 2 ml of triethylamine were added to a stirred solution of 2.01 g of 6,7,8,9-tetrahydropyrido[1,2-a]indole-8-methanol in 40 ml of dichloromethane under a nitrogen atmosphere. After 18 hours, the mixture was washed with saturated sodium bicarbonate solution, dried and evaporated to an oil. Then, 1.8 g of this oil were dissolved in 10 ml of isopropanol and 5 ml of 33% aqueous ammonia and the mixture was heated to 80° C. for 10 hours. The solvent was removed under reduced pressure and the residue was partitioned between dichloromethane and saturated sodium bicarbonate solution. The organic phase was dried and evaporated to give 1.3 g of 8-aminomethyl-6,7,8,9-tetrahydropyrido[1,2-a]indole of melting point 85°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721245
Source datasetuspto-grants-1998_02
ORD IDord-4223f1a63c434a9faadaa7c65c19b2d7
Source noteuspto-grants-1998_02