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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874736Generated: October 30, 2026

Diisopropylethylamine → HCID 178523100, compound

https://huagongshe.com/reaction/874736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactantcyclopropyl(1,3-thiazol-2-yl)methanamineHCID 46785163—
ReactantHCID 178524181HCID 178524181—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178523100HCID 17852310052.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound was synthesized according to General Method A utilizing 3-iodo-1H-indazole-5-carboxylic acid (255 mg, 0.88 mmol), cyclopropyl(thiazol-2-yl)methanamine (150 mg, 0.97 mmol), TBTU (310 mg, 0.97 mmol), DIPEA (0.31 mL, 1.8 mmol), and DMF (8 mL). The reaction was stirred at 0° C. for 1 h. The crude reaction was subsequently diluted with H2O. A filtration and washing (H2O) of the precipitate provided the desired product as a beige solid (195 mg, 52%). The product used without further purification. 1H NMR (400 MHz, CD3OD) δ ppm 8.16 (br. s., 1H), 7.99 (m., 1H), 7.77 (br. s., 1H), 7.46-7.67 (m, 2H), 1.45-1.68 (m, 1H), 0.46-0.90 (m, 4H); MS ESI 425.0 [M+H]+, calcd for [C15H13IN4OS+H]+ 425.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980934B2
Source datasetuspto-grants-2015_03
ORD IDord-bde75df797a34269bbae75374c7924f0
Source noteuspto-grants-2015_03