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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588493Generated: October 31, 2026

Dimethyl Sulfoxide → 5-((1R)-1-{[(tert-butylamino)carbonyl]amino}ethyl)-N-hydroxythiophene-2-carboxamide

https://huagongshe.com/reaction/588493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl isocyanateHCID 62412—
ReactantO-(tert-Butyldimethylsilyl)hydroxylamineHCID 4691350—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(R)-4-(1-aminoethyl)benzoic acid hydrochlorideHCID 67395329—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-((1R)-1-{[(tert-butylamino)carbonyl]amino}ethyl)-N-hydroxythiophene-2-carboxamideHCID 5337404835%

Reaction Steps

To the vial containing (R)-4-(1-aminoethyl)benzoic acid hydrochloride from Step 1 was added tert-butyl isocyanate (0.026 mL, 0.23 mmol), N,N dimethylformamide (2.5 mL) and triethylamine (0.21 mL, 1.50 mmol). After the reaction was stirred at rt for 16 h, HATU (0.057 g, 0.150 mmol) in N,N-dimethylformamide (0.5 mL) was added, immediately followed by the addition of O-(tert-butyldimethylsilyl)hydroxylamine (0.0331 g, 0.225 mmol) in DCM (1.0 mL). This mixture was shaken at rt for 1 hr after which it was evaporated to dryness. To the resulting residue was added hydrochloric acid (4 mL, 1% in IPA). After shaking at rt for 30 min, solid NaHCO3 was added to quench excess acid and the solvent was then completely evaporated to dryness to give a solid residue. This solid was dissolved in DMSO (1.2 mL), and the solution was filtered and purified via Gilson prep-HPLC to give the title compound (0.015 g, 35%) as a white solid. LC-MS: (FA) ES+ 286; 1H NMR (Methanol-d4, 300 MHz) δ 7.41 (m, 1H), 6.91 (d, J=4.7 Hz, 1H), 5.03 (q, J=6.8 Hz, 1H), 2.03 (m, 4H), 1.96 (m, 8H), 1.69 (m, 8H), 1.47 (d, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227951B2
Source datasetuspto-grants-2016_01
ORD IDord-6d5cd798d22040e0bba0a5cfc91e0a28
Source noteuspto-grants-2016_01