Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 68459548 | HCID 68459548 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178465594 | HCID 178465594 | — |
Reaction Steps
C-(7-Benzenesulfonyl-chroman-4-yl)-methylamine HCl salt (90 mg, 0.26 mmol) and methyl imidate (acetimidic acid methyl ester, 58 mg, 0.529 mmol) were dissolved in 3 mL of absolute ethanol and 0.362 mL of triethylamine (2.6 mmol) was added. The reaction mixture was stirred at 80° C. for 2 days. It was then cooled, partitioned between EtOAc and water, dried over MgSO4 concentrated and purified using column chromatography (silica gel, MeOH/CHCl3/NH4OH 10:89:1) After formation of the HCl salt, 9 mg (10%) of. N-(7-Benzenesulfonyl-chroman-4-ylmethyl)-acetamidine was collected. MS: 345 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759389B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d22973542ede448ab01c3e5e14a14730 |
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| Source note | uspto-grants-2010_07 |
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