Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49732Generated: October 30, 2026

3-((Furan-2-ylmethyl)amino)propanenitrile → HCID 178429056, compound

https://huagongshe.com/reaction/49732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-((Furan-2-ylmethyl)amino)propanenitrileHCID 2063331—
ReactantHCID 139887068HCID 139887068—
ProductHCID 178429056HCID 17842905649%

Reaction Steps

N,N′-Bis-(tert-butoxycarbony)-3-[5-methyl-3-(2-(N-(2-cyanoethyl)-N-(2-furanylmethyl)aminosulfonyl)phenylsulfonyloxy)phenoxy]propoxyguanidine: The title compound was prepared in 49% yield from 3-(furfurylamino)propionitrile, in a manner analogous to step h of Example 20. 1H NMR (300 MHz, CDCl3) δ 9.08 (s, 1H), 8.29 (dd, 1H, J=7.9, 1.4 Hz), 8.16 (dd, 1H, J=7.8, 1.5 Hz), 7.79 (m, 1H), 7.70 (m, 2H), 7.33 (t, 1H, J=1.3 Hz), 6.60 (m, 1H), 6.57 (m, 1H), 6.52 (t, 1H, J=2.1 Hz), 6.32 (m, 2H), 4.65 (s, 2H), 4.18 (t, 2H, J=6.2 Hz), 3.94 (t, 2H, J=6.2 Hz), 3.65 (m, 2H), 2.55 (m, 2H), 2.24 (s, 3H), 2.10 (pentet, 2H, J=6.2 Hz), 1.49 (s, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706765B2
Source datasetuspto-grants-2004_03
ORD IDord-42e4a90585a7403880f41ff86927aae9
Source noteuspto-grants-2004_03