HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234294Generated: October 30, 2026
p-Toluenesulfonic acid monohydrate → HCID 68685078, compound
https://huagongshe.com/reaction/2234294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Amino-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide | HCID 11529063 | — |
| Reactant | HCID 86617547 | HCID 86617547 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 4-Methyl-2-Pentanol | HCID 7910 | — |
| Product | HCID 68685078 | HCID 68685078 | 20.1% |
Reaction Steps
10-chloro-2-(1-methoxypropan-2-yl)-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-one (Intermediate 137; 35 mg, 0.13 mmol)), 4-amino-3-methoxy-N-(1-methyl-4-piperidyl)benzamide (WO06/018220; 34 mg, 0.13 mmol) and p-toluenesulphonic acid monohydrate (61 mg, 0.32 mmol) were dissolved in 4-methyl-2-pentanol (2 mL) and heated at 100° C. for 18 hrs. The reaction mixture was cooled to room temperature dissolved in MeOH and added to a 2 g SCX-2 column pre wet with MeOH (2 column volumes). Flushed with MeOH (2 column volumes) and the product eluted with 2M ammonia in MeOH. Product containing fractions were evaporated and the resultant material purified by base modified reverse phase HPLC to yield the title compound as a cream coloured solid (13 mg, 20%)
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-da3e425c924b4e67bb92940e2dddcba7 |
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| Source note | uspto-grants-2010_05 |
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