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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467914Generated: November 2, 2026

HCID 61624701, compound → HCID 86691616, compound

https://huagongshe.com/reaction/1467914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 61624701HCID 61624701—
ReactantHCID 86691617HCID 86691617—
SolventDichloromethaneHCID 6344—
ProductHCID 86691616HCID 86691616100%

Reaction Steps

Intermediate 74 2[(3-isothiocyanato-1H-pyrazol-1-yl)methyl]-6-methylpyridine (101 mg, 0.439 mmol) was dissolved in 4 mL of DCM, and then Intermediate 102 2-(3,5-dimethyl-1H-pyrazol-1-yl)propanohydrazide (80 mg, 0.439 mmol) was added. The mixture was stirred at room temperature for 2 h. Solvent was evaporated under vacuum to give 2-[2-(3,5-dimethyl-1H-pyrazol-1-yl)propanoyl]-N-{1-[(6-methyl-2-pyridinyl)methyl]-1H-pyrazol-3-yl}hydrazinecarbothioamide (181 mg, 0.439 mmol, 100% yield) as yellow solid. [ES+MS] m/z 413 (MH+)]. Solid was dissolved in 5 mL of POCl3 and the mixture was stirred at 100° C., until no starting material was detected (1 h 30 minutes). Crude of reaction was partitioned between DCM and distilled water. Organic layer was dried over MgSO4 (anh), filtered and concentrated to give a light yellow solid. This solid was purified by HPLC preparative using X-Terra chromatography column (30 mm×150 mm), gradient 0% to 40% ACN/H2O, in neutral conditions to yield the title compound as a white solid (22 mg, 12.7%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 10.87 (br s, 1H), 7.77 (d, 1H), 7.59-7.65 (m, 1H), 7.15-7.17 (m, 1H), 6.77-6.80 (m, 1H), 6.01 (d, 1H), 5.83 (br s, 1H), 5.77 (q, 1H), 5.26 (s, 2H), 2.45 (s, 3H), 2.24 (s, 3H), 2.08 (s, 3H), 1.78 (d, 3H). [ES+MS] m/z 395 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000181B2
Source datasetuspto-grants-2015_04
ORD IDord-dcb15d1563c649cb920c265773035e4e
Source noteuspto-grants-2015_04