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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038052Generated: October 31, 2026

1,2-Dichloroethane → HCID 24763146, compound

https://huagongshe.com/reaction/2038052

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(1,3-Dioxaindan-5-yl)cyclopropane-1-carboxylic acidHCID 14349608—
ReactantHCID 59129351HCID 59129351—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 24763146HCID 2476314694.2%

Reaction Steps

tert-Butyl 2-(5-amino-1H-indol-2-yl)-2-methylpropylcarbamate (58 mg, 0.19 mmol), 1-(benzo[d][1,3]dioxol-6-yl)cyclopropanecarboxylic acid (47 mg , 0.23 mmol), EDC (45 mg, 0.23 mmol), HOBt (31 mg, 0.23 mmol) and Et3N (80 μL, 0.57 mmol) were dissolved in DMF (4 mL) and stirred overnight at room temperature. The mixture was diluted with water and extracted with ethylacetate. The combined organic phases were dried over magnesium sulfate and evaporated to dryness. The residue was purified by silica gel chromatography (10-30% ethylacetate in hexane) to give tert-butyl 2-(5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indol-2-yl)-2-methylpropyl-carbamate (88 mg, 94%). 1H NMR (400 MHz, CDCl3) δ 8.32(s, 1H), 7.62(d, J=1.5 Hz, 1H), 7.18-7.16(m, 2H), 7.02-6.94(m, 3H), 6.85(d, J=7.8 Hz, 1H), 6.19(d, J=1.5 Hz, 1H), 6.02(s, 2H), 4.54(m, 1H), 3.33 (d, J=6.2 Hz, 2H), 1.68(dd, J=3.7, 6.8 Hz, 2H), 1.36(s, 9H), 1.35(s, 6H), 1.09(dd, J=3.7, 6.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575209B2
Source datasetuspto-grants-2013_11
ORD IDord-032bf370c7674ff79875d87b9a18a348
Source noteuspto-grants-2013_11