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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742872Generated: October 25, 2026

Tert.butyl 2-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/742872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert.butyl 2-benzyloxycarbonyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 86746252—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductTert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 8674625377.5%

Reaction Steps

1.62 g of tert.butyl 2-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 numberUS05554756
Source datasetuspto-grants-1996_09
ORD IDord-79ea7faf46dd438f8a7607c920cf157e
Source noteuspto-grants-1996_09