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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427174Generated: October 30, 2026

HCID 86753660, compound → HCID 178496046, compound

https://huagongshe.com/reaction/427174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86753660HCID 86753660—
ReactantHCID 178496047HCID 178496047—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178496046HCID 17849604661.8%

Reaction Steps

The intermediate tert-butyl N-(3-((2-methoxyacetimidoyl) aminomethyl)benzyl)carbamate (360 mg) prepared from tert-butyl N-(3-(aminomethyl)benzyl carbamate and intermediate G analogous to example 1 was deprotected in trifluoroacetic acid at 20° C. for 16 h. The crude product was purified by C18 reverse phase chromatography eluting with water (0.1% trifluoroacetic acid) to yield 150 mg of N-(3-(Aminomethyl)benzyl)-2-methoxyacetamidine as a yellowed, viscous oil (freeze-dried). Mass spectrum (CI) 208.0 (MH+, 100%). 1H NMR (200 MHz, D2O) δ 7.5-7.3 (m, 4H), 4.57 (s, 2H), 4.37 (s, 2H), 4.15 (s, 2H), 3.44 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037438E1
Source datasetuspto-grants-2001_11
ORD IDord-d355283def344428b46a6ffae78127c2
Source noteuspto-grants-2001_11