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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189242Generated: October 30, 2026

Thiosemicarbazide → HCID 136068476, compound

https://huagongshe.com/reaction/2189242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiosemicarbazideHCID 2723789—
ReactantHCID 86761715HCID 86761715—
SolventEthanolHCID 702—
ProductHCID 136068476HCID 136068476—

Reaction Steps

(S)-tert-Butyl 3-(2-(5-formyl-2-methoxyphenyl)quinazolin-4-ylamino)pyrrolidine-1-carboxylate (0.160 g, 0.357 mmol) was dissolved in ethanol (2 mL) and thiosemicarbazide (0.033 g, 0.362 mmol) was added and the solution was stirred at room temperature for 16 h. The solid was filtered off and washed with ethanol (2×1 mL). The solid was suspended in water (16 mL) and ferric chloride (0.267 g, 1.00 mmol) was added and the solution was heated at 60° C. for 16 h. A further portion of ferric chloride (0.267 g, 1.00 mmol) was added and the solution heated at 90° C. for 2.5 h. The reaction mixture was partitioned between water (20 mL) and dichloromethane (20 mL), but the bright yellow product was visibly in the aqueous phase so the aqueous phase was concentrated in vacuo and the residue was purified by ion exchange chromatography on SCX-2 (solute acidic resin (2 g), eluting with methanol and then 1 M ammonia in methanol. The basic fractions were combined and purified by HPLC. Semi-prep HPLC was performed on an Agilent 1200 series with a Phenomex Gemini 250 mm×10 mm i.d. column at a temperature of 20 C and a flow rate of 5 mL/min using a gradient of 10%-100% acetonitrile in water over 30 mins.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324226B2
Source datasetuspto-grants-2012_12
ORD IDord-658ae5c3da2b4ddd84fa3f33681d7e4f
Source noteuspto-grants-2012_12