HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309656Generated: October 30, 2026
Ethyl 2-isothiocyanatobenzoate → HCID 14013538, compound
https://huagongshe.com/reaction/2309656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-isothiocyanatobenzoate | HCID 523235 | — |
| Reactant | HCID 14013481 | HCID 14013481 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14013538 | HCID 14013538 | 18.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04695575 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-0b3b476bd43b4ede9260397a78505679 |
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| Source note | uspto-grants-1987_09 |
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