Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382042Generated: October 27, 2026

Dimethylformamide → 4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol

https://huagongshe.com/reaction/2382042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-olHCID 68559083—
Product4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-olHCID 68552158—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of NaH (8.1 g, 204 mmol, 60% in mineral oil) in DMF (100 mL) at 0° C. is treated with 4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol (3 g, 13.6 mmol) and stirred at 0° C. for 0.5 h. The mixture is treated with HOSA (7.7 g, 68 mmol) portion wise and warmed to rt over 2 h. The mixture is then poured over ice, filtered through a pad of Celite, and extracted with EtOAc (3×100 mL). The combined organic layer is dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by filtration through a short plug of silica gel to afford 4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol, which is used in the next step without further purification. MS: 237 (M+H); 1H NMR (300 MHz, CDCl3): δ 7.30 (m, 1H), 7.22 (m, 1H), 6.98 (m, 2H), 4.71 (s, NH2, 2H), 2.75 (m, 2H), 1.86 (m, 2H), 1.31 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-070c0434271c486baca24c458aba37cd
Source noteuspto-grants-2012_09