N,O-Dimethylhydroxylamine → HCID 86671822, compound

Participants

Role	Name	HCID	Charge
Reactant	N,O-Dimethylhydroxylamine	HCID 14232	—
Reactant	Diisopropylethylamine	HCID 81531	—
Reactant	Cyclobutanecarboxylic acid, 1-(((1,1-dimethylethoxy)carbonyl)amino)-	HCID 1512646	—
Reactant	Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)	HCID 9886157	—
Solvent	Dimethylformamide	HCID 6228	—
Product	HCID 86671822	HCID 86671822	87%

Reaction Steps

To a solution of 1-tert-butoxycarbonylamino-cyclobutanecarboxylic acid (3 g, 13.94 mmol) in dry DMF (50 mL) was added N,O-dimethylhydroxylamine x HCl (1.36 g, 13.94 mmol) and DIEA (9.21 mL, 55.75 mmol). The reaction flask was cooled to 0° C. and after 10 minutes HATU (5.30 g, 13.94 mmol) was added to the solution (which turned yellow on addition). After 2 hrs the DMF was removed by rotary evaporation at reduced pressure. The residue was dissolved in EtOAc (100 mL) and washed twice with 10% citric acid (aq) and saturated NaHCO3(aq) solution. The organic phase was dried with Na2SO4, filtered and evaporated on silica. The product was purified by flash chromatography (heptane: ethyl acetate (1:1) to give the product as a colourless oil that slowly crystallizes (3.13 g) in 87% yield.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US08859605B2
Source dataset	uspto-grants-2014_10
ORD ID	ord-cc2b44842334443cae2b9a779cdf8194
Source note	uspto-grants-2014_10