HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234345Generated: October 31, 2026
p-Toluenesulfonic acid monohydrate → HCID 68685529, compound
https://huagongshe.com/reaction/2234345
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-Chloro-9-cyclopentyl-5-methyl-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-one | HCID 57940526 | — |
| Reactant | HCID 68685990 | HCID 68685990 | — |
| Solvent | 4-Methyl-2-Pentanol | HCID 7910 | — |
| Product | HCID 68685529 | HCID 68685529 | 23.1% |
Reaction Steps
p-Toluenesulphonic acid monohydrate (338 mg, 1.78 mmol) was added to 4-amino-2,5-difluoro-N-[(1S,5R)-9-methyl-9-azabicyclo[3.3.1]non-7-yl]benzamide (Intermediate 274; 220 mg, 0.71 mmol), and 2-chloro-9-cyclopentyl-5-methyl-8,9-dihydro-5H-pyrimido[5,4-b][1,4]diazepin-6(7H)-one (Intermediate 1; 200 mg, 0.71 mmol) in 4-methyl-2-pentanol (4 mL) at 25° C. The resulting mixture was heated by microwave irradiation at 150° C. for 1 hour. The crude product was purified by ion exchange chromatography, using an SCX-3 (5 g) column. The desired product was eluted from the column using 2M NH3/MeOH and product-containing fractions were evaporated to dryness. The residue was further purified by base modified reverse phase preparative HPLC to yield the title compound as a white solid (91 mg, 23.%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709471B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-cff955e01cf74d60ac99e399f915eac3 |
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| Source note | uspto-grants-2010_05 |
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