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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038083Generated: October 31, 2026

Acetyl chloride → HCID 59129222, compound

https://huagongshe.com/reaction/2038083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 59129249HCID 59129249—
SolventDimethylformamideHCID 6228—
ProductHCID 59129222HCID 59129222—

Reaction Steps

To a solution of N-(1-(2-aminoethyl)-2-tert-butyl-6-fluoro-1H-indol-5-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropane-carboxamide (47 mg, 0.10 mmol) and Et3N (28 μL, 0.20 mmol) in DMF (1 mL) was added acetyl chloride (7.1 μL, 0.10 mmol). The mixture was stirred at room temperature for 1 h before being filtered and purified by reverse phase HPLC (10-99% CH3CN/ H2O) to yield N-(1-(2-acetamidoethyl)-2-tert-butyl-6-fluoro-1H-indol-5-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide. 1 H NMR (400 MHz, DMSO-d6) δ8.35(s, 1H), 8.15(t, J=5.9 Hz, 1H), 7.53(s, 1H), 7.43-7.31(m, 4H), 6.17(s, 1H), 4.22(m, 2H), 3.30(m, 2H), 1.85(s, 3H), 1.47(m, 2H), 1.41(s, 9H), 1.13(m, 2H). HPLC ret. time 2.06 min, 10-99% CH3CN, 3 min run; ESI-MS 516.4 m/z (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575209B2
Source datasetuspto-grants-2013_11
ORD IDord-b50fb90c76bf49e9bbba05bc8372d2e8
Source noteuspto-grants-2013_11