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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640986Generated: November 1, 2026

Diisopropylethylamine → HCID 66737367, compound

https://huagongshe.com/reaction/1640986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66737151HCID 66737151—
ReactantHCID 86643841HCID 86643841—
SolventDiethyl EtherHCID 3283—
ProductHCID 66737367HCID 6673736770%

Reaction Steps

To a mixture of 5-(3-fluoro-benzenesulfonyl)-1-trityl-1H-indazol-3-ylamine (100 mg, 0.187 mmol), N,N-diisopropylethylamine (0.13 mL, 0.75 mmol) and dry-tetrahydrofuran (30 mL), at room temperature, was added 4-(4-methyl-piperazin-1-yl)-2-nitro-benzoyl chloride hydrochloride (66 mg, 0.206 mmol, prepared as described in Example 20). The mixture was stirred at room temperature for 1 hour then evaporated to dryness. The residue was dissolved in dichloromethane (50 mL), washed with saturated solution of sodium hydrogenocarbonate (50 mL), dried over sodium sulfate, evaporated to dryness and triturated with diethylether affording the title compound as a yellow powder (102 mg, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114865B2
Source datasetuspto-grants-2012_02
ORD IDord-0e2142488f8a436ebcbca4d25da2fb50
Source noteuspto-grants-2012_02