Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080301Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 57542846, compound

https://huagongshe.com/reaction/2080301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 51557285HCID 51557285—
ReactantHCID 57542598HCID 57542598—
SolventDimethylformamideHCID 6228—
ProductHCID 57542846HCID 57542846—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 5-fluoro-2-(3-fluorophenethylamino)-6-(1-methyl-1H-pyrazol-4-yl)nicotinic acid (14.3 g, 40 mmol) and DMF (300 mL) was added of HBTU (18.2 g, 48 mmol) and HOBT (6.49 g, 48 mmol). The mixture was cooled down to 0° C., 8.93 g (48 mmol) of (R)-tert-butyl 2-(aminomethyl)azetidine-1-carboxylate was added, followed by 13.9 ml of DIEA (80 mmol). The mixture was stirred at r.t for 1 hour and extracted with 300 mL EtOAc. The organic layer was washed with 500 mL brine, dried over MgSO4 and then concentrated. The residue was purified by Biotage silica gel chromatography using EtOAc:Hex (1:1) as eluant. (R)-tert-butyl 2-((5-fluoro-2-(3-fluorophenethylamino)-6-(1-methyl-1H-pyrazol-4-yl)nicotinamido)methyl)azetidine-1-carboxylate was obtained as a yellow solid (16.5 g, yield 80%). LRMS (M+H+) m/z 527.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932270B2
Source datasetuspto-grants-2011_04
ORD IDord-40f9b29587e440c1b8808e416219e7fa
Source noteuspto-grants-2011_04