Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855410Generated: October 28, 2026

Diisopropylethylamine → HCID 11570025, compound

https://huagongshe.com/reaction/855410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-chloro-6-fluoro-1H-indole-7-carboxylic acidHCID 25113647—
Reactant(4-Tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amineHCID 68576819—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11570025HCID 1157002536.6%

Reaction Steps

To a solution of 100 mg (0.47 mmol) of 5-chloro-6-fluoro-1H-indole-7-carboxylic acid and 150 mg of TBTU (0.47 mmol) in 10 ml DMF, were added 0.4 ml (2.34 mmol) of N,N-diisopropylethyl amine. After stirring for 5 min at rt, 156 mg (0.47 mmol) of (4-tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amine were added. After stirring for 22 h at rt, the reaction mixture was diluted with 10 ml water and extracted with EtOAc (2×). The combined organic phases were washed with water and brine, dried with magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by two successive column chromatographies (8 g silica gel; EtOAc/heptane 1:3; then again 8 g silica gel; and DCM/heptane 70:30 to 90:10) to give 91 mg white solid (27%). MS(ISP) 528.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-f2f737f912b84ffdb70eb79994a10f60
Source noteuspto-grants-2007_08