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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73704Generated: October 27, 2026

Formaldehyde → 6-Methyl-7-(1,4-oxazepan-4-ylmethyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine

https://huagongshe.com/reaction/73704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,4-Oxazepane hydrochlorideHCID 23090214—
Reactant6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 55288621—
SolventAcetic AcidHCID 176—
Product6-Methyl-7-(1,4-oxazepan-4-ylmethyl)pyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 5795521078%

Reaction Steps

A solution of formaldehyde (0.61 mL, 8.10 mmol, 37% in H2O) and homomorpholine hydrochloride (1.11 g, 8.10 mmol) in AcOH (5 mL) was added to a stirring solution of 6-methylpyrrolo[2,1-f][1,2,4]triazin-4-amine (1.00 g, 6.75 mmol) in AcOH (5 mL) at 60° C. The reaction was allowed to stir until all starting material had been consumed as shown by HPLC (1 hr). The reaction mixture was worked up by diluting with EtOAc and washing 3× with saturated sodium carbonate solution. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude product was triturated with Et2O to obtain 1.37 g (78%) of a light brown powder. 1H-NMR (DMSO-d6) δ 7.76 (s, 1H), 7.47 (br s, 2H), 6.65 (s, 1H), 3.85 (s, 2H), 3.62 (t, J=5.7 Hz, 2H), 3.55-3.51 (m, 2H), 2.61-2.55 (m, 4H), 2.21 (s, 3H), 1.77-1.74 (m, 2H); MS [M+H]+=262.0; LCMS RT=1.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829185B2
Source datasetuspto-grants-2014_09
ORD IDord-72629167bff4445686cb3d7e42dc5442
Source noteuspto-grants-2014_09