Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 3006320 | HCID 3006320 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 508624 | HCID 508624 | 65% |
Reaction Steps
To a stirred solution of thioamide Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nα-[N′α-(4-methylbenzenesulfonyl)-L-thiotryptophanyl]-L-lysine (240 mg, 0.33 mmol, example 73) in MeOH (3 mL) was added cyanamide (28 mg, 0.66 mmol). The mixture was stirred for 5 min, then mercuric acetate (209 mg, 0.66 mmol) was added. The reaction was stirred for 3 h then diluted with saturated NH4Cl and extracted with EtOAc. The organic layer was washed with brine and concentrated then rediluted with THF/MeOH (2 mL/1 mL) and treated with 1N NaOH (0.8 mL). After stirring for 4 h, the reaction was acidified with 1N HCl and extracted with EtOAc. The organic layer was dried over MgSO4, concentrated and purified by column chromatography to give 154 mg (65%) of the final product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608100B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-1feb8c067cba464e90ef21655be24e04 |
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| Source note | uspto-grants-2003_08 |
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