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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094230Generated: November 1, 2026

Isopropylamine → HCID 24803615, compound

https://huagongshe.com/reaction/2094230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantCyanogen BromideHCID 10476—
ReactantHCID 59216810HCID 59216810—
SolventAcetic AcidHCID 176—
ProductHCID 24803615HCID 24803615—

Reaction Steps

A 35 mL scintillation vial was charged with 4-chloro-N-(5-chloro-2-(hydrazinecarbonyl)pyridine-3-yl)-3-(trifluoromethyl)benzenesulfonamide (500 mg, 1.1 mmol), cyanogenbromide (200 mg, 2.0 mmol) anhydrous MeCN (5 mL). The resultant mixture was heated to 65° C. and stirred for 2 h. After cooling to room temperature, isopropylamine (500 mg, 8.2 mmol) was added followed by AcOH (0.5 mL) and the mixture was heated to 135° C. and stirred for 2 h. After cooling to room temperature, reaction mixture was concentrated under reduced pressure. The residue was further purified through automated normal-phase chromatography (10% to 100% gradient of EtOAc-Hexane) and followed by preparative HPLC (10% to 90% gradient of MeCN-water) and dried (Lyophilizer) to afford the title compound. 1H NMR (400 MHz, CDCl3) 8.28 (d, 1H), 8.18 (d, 1H), 8.10 (d, 1H), 7.90 (dd, 1H), 7.58 (d. 1H), 4.32 (br, 1H), 3.88 (m, 1H), 1.34 (d (d, 6H). MS (ES) [M+H]+ expected 495.0. found 495.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445518B2
Source datasetuspto-grants-2013_05
ORD IDord-e1b34f500f494935a3026ddfee362f9f
Source noteuspto-grants-2013_05