HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652184Generated: October 29, 2026
Methyl isothiocyanate → HCID 14183054, compound
https://huagongshe.com/reaction/652184
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | HCID 22397358 | HCID 22397358 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14183054 | HCID 14183054 | 55.1% |
Reaction Steps
A stirred mixture of 4-[1-(4-fluorophenyl)-1H-indazol-3-yl]piperidine-1-carbonitrile of Example 102 (30 g, 0.094 moles) and 25% H2SO4 (225 ml) was refluxed for 20 hours. The mixture was cooled, poured into H2O, and basified with a 25% NaOH solution. The product was extracted (dichloromethane), dried (MgSO4), and concentrated to yield 21 g (76%) of 1-(4-fluorophenyl)-3-(4-piperidinyl)-1H-indazole as an oil. To a stirred suspension of the indazole (4.0 g, 0.0135 moles) in toluene (70 ml) was added dropwise methyl isothiocyanate (1.5 ml, 0.022 moles). The mixture was stirred for 23 hours at ambient temperature during which time the product precipitated from the solution. The product was collected and recrystallized twice from isopropyl alcohol to yield 2.74 g (55%) of N-methyl-4-[1-(4-fluorophenyl)-1H-indazol-3-yl]piperidine-1-carbothioamide, m.p. 179°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670447 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-72ec00310da442fbb7871405a2c31ff0 |
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| Source note | uspto-grants-1987_06 |
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