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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309656Generated: October 30, 2026

Ethyl 2-isothiocyanatobenzoate → HCID 14013538, compound

https://huagongshe.com/reaction/2309656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-isothiocyanatobenzoateHCID 523235—
ReactantHCID 14013481HCID 14013481—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14013538HCID 1401353818.6%

Reaction Steps

To a stirred mixture of 5.1 parts of 4-[[3-(2-furanylmethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperidineethanamine and 270 parts of tetrahydrofuran was added dropwise a solution of 3.8 parts of ethyl 2-isothiocyanatobenzoate in tetrahydrofuran. Upon completion, stirring was continued for 1 hour. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanone. The product was filtered off and dried, yielding 1.4 parts (18.6%) of 3-[2-[4-[[3-(2-furanylmethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperidinyl]ethyl]-2,3-dihydro-2-thioxo-4(1H)-quinazolinone; mp. 192.0° C. (492).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-0b3b476bd43b4ede9260397a78505679
Source noteuspto-grants-1987_09