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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500807Generated: October 27, 2026

Formaldehyde → tert-Butyl 4-[(4-amino-6-methylpyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1500807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 55288621—
SolventAcetic AcidHCID 176—
Producttert-Butyl 4-[(4-amino-6-methylpyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]piperazine-1-carboxylateHCID 86687876105%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 6-methylpyrrolo[2,1-f][1,2,4]triazin-4-amine (500 mg, 3.3 mmol; preparation described in PCT Int. Pat. Appl. WO 2007/056170) in acetic acid (8 ml) was treated with 37% aq. formaldehyde solution (328 μl, 4.04 mmol) and tert-butyl piperazine-1-carboxylate (754 mg, 4.04 mmol). The mixture was stirred at 60° C. overnight. After evaporation, the residue was taken up in ethyl acetate and washed with sat. aq. sodium hydrogencarbonate solution. The aqueous layer was extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulfate and evaporated affording 1.2 g of the crude product which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206184B2
Source datasetuspto-grants-2015_12
ORD IDord-4a30e75a1d6c4eeaafd74b6a7c99a20c
Source noteuspto-grants-2015_12