Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 68162930 | HCID 68162930 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86669245 | HCID 86669245 | — |
Reaction Steps
1,1-Dimethylethyl 4-({4-[(cis)-1-acetyl-2-methyl-4-({[(1-methylethyl)oxy]carbonyl}amino)-1,2,3,4-tetrahydro-6-quinolinyl]phenyl}methyl)hexahydro-1H-1,4-diazepine-1-carboxylate (for a preparation see Intermediate 11) (78 mg, 0.135 mmol) was dissolved in methanol (3 mL) and to this was added 1.25M HCl in methanol (1 mL, 1.250 mmol). The reaction vessel was sealed and heated in Emrys Optimiser microwave to 70° C. for 2 hr. After cooling the reaction was reduced in vacuo to give a colourless solid and placed under high vacuum for 1 hr. Transferred to vial using methanol, reduced, and then redissolved in ether to give a colourless solid (66 mg). LCMS (Method A): Rt=0.96, MH+=479
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697725B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-87e1eca2ecf0494db844e16fc9024e7c |
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| Source note | uspto-grants-2014_04 |
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