Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 10327519 | HCID 10327519 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 68825644 | HCID 68825644 | — |
Reaction Steps
2.0 g (2.6 mmol) (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-1-[4-(4-methyl-piperazin-1-yl)-piperidin-1-yl]-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butane-1,4-dione are dissolved in 20 ml isopropanol and at 50° C. combined with 0.6 ml hydrobromic acid (47% in water). The mixture is cooled to 4° C. within 30 minutes. The solid formed is filtered off, washed with 5 ml cold isopropanol and dried for 12 hours at 40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638625B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-6c1adfd3480c41099f2fbbf32f9b97cc |
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| Source note | uspto-grants-2009_12 |
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