Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54086Generated: October 25, 2026

Tert.butyl-benzyloxycarbonyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide → Tert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide

https://huagongshe.com/reaction/54086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert.butyl-benzyloxycarbonyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 86750718—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductTert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 86746253155%

Reaction Steps

1.62 g of tert.butyl-benzyloxycarbonyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide were dissolved in 10 ml of a 45% solution of hydrogen bromide in acetic acid. After 30 minutes the solution was evaporated and the residue was taken up in water. After filtration the filtrate was washed three times with diethyl ether and then neutralized by the addition of saturated aqueous sodium bicarbonate solution. The product was extracted from the now turbid aqueous layer with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated to give 0.84 g of tert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide as a white crystalline solid of melting point 144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620987
Source datasetuspto-grants-1997_04
ORD IDord-a4977fe4b1a4413ca21a06675e7a8fb3
Source noteuspto-grants-1997_04