HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616700Generated: November 1, 2026
Benzoyl isothiocyanate → HCID 86731951, compound
https://huagongshe.com/reaction/1616700
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | HCID 86731952 | HCID 86731952 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86731951 | HCID 86731951 | 34.2% |
Reaction Steps
To a solution of tert-butyl 2-amino-5-methyl-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate (0.104 g, 0.386 mmol, 1 eq) in dry ethanol (1 mL) under argon was added benzoyl isothiocyanate (0.15 mL, 1.08 mmol, 2.8 eq). The mixture was heated at reflux for 16 hours. The solvent was evaporated in vacuo. Purification by reverse-phase chromatography (10-100% CH3CN: Water ramp over 20 min) afforded the desired product tert-butyl 2-(3-benzoylthioureido)-5-methyl-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate as a pale yellow oil (0.057 g, 0.132 mmol, 34% yield). 1H NMR (400 MHz, DMSO) δ 14.72 (s, 1H), 11.89 (s, 1H), 8.06-7.95 (m, 2H), 7.69 (t, J=7.4, 1H), 7.57 (t, J=7.7, 2H), 4.78 (d, J=14.8, 1H), 4.66 (d, J=15.0, 1H), 3.80-3.63 (m, 1H), 2.93 (d, J=16.7, 1H), 2.50-2.44 (m, 1H), 1.59 (s, 9H), 1.30 (d, J=6.1, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765803B1 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-37dbe6f006be48b3923e30be9d733bdb |
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| Source note | uspto-grants-2014_07 |
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