HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160107Generated: October 28, 2026
HCID 11327446, compound → HCID 11361452, compound
https://huagongshe.com/reaction/1160107
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 11327446 | HCID 11327446 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11361452 | HCID 11361452 | 94% |
Reaction Steps
To a 10 mL recovery flask was added 2-(2-amino-5-cyano-6-methylsulfanyl-pyrimidin-4-ylsulfanyl)-N-(2-amino-5-trifluoromethyl-phenyl)-acetamide (and regioisomer) (10 mg, 0.0241 mmol) and AcOH (2 mL). The solution was stirred at 120° C. for 1 h. The reaction mixture was concentrated. The resulting film was resuspended in 1:1 CH3CN/H2O and lyophilized to give 2-amino-4-methylsulfanyl-6-(6-trifluoromethyl-1H-benzoimidazol-2-ylmethylsulfanyl)-pyrimidine-5-carbonitrile as a tan powder (9 mg, 94%). LC/MSD (HP Series 1100 MSD) Expected MW: 396.04, Observed M+H, 397.0, Retention time: 1.49. Analytical LC: 98%, Retention time: 4.46 (11 minute run). 1H-NMR, DMSO-d6, Varian 400 MHz δ 12.69 (m, 1H), 8.10 (bs, 1H), 7.91-7.79 (d, 1H), 7.76-7.64 (dd, 1H), 7.51-7.46 (dd, 1H), 4.68 (s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816353B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-4e4fdd762f304713919d7979c74132f8 |
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| Source note | uspto-grants-2010_10 |
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