HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379852Generated: November 1, 2026
Hydrochloric Acid → HCID 131720218, compound
https://huagongshe.com/reaction/1379852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22877438 | HCID 22877438 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131720218 | HCID 131720218 | 96% |
Reaction Steps
To a solution of 9.83 g (0.55 mmol) of 2-benzyloxycarbonylamino-2-methyl- N-[2,3,4,5-tetrahydro-2-oxo-1-[[2'-[(t-butoxycarbonylamino)methyl][1,1'-biphenyl]-4-yl]methyl]-1H-benzazepin-3(R)-yl]propanamide (Step H) in 170 mL of methanol was added 120 mL of 9 N aqueous hydrochloric acid. Periodically 10 mL portions of methanol were added to the reaction mixture to dissolve precipitates which form during the reaction (50 mL total). The reaction mixture was stirred overnight at room temperature then the solvent was removed under vacuum. The resulting oil was dissolved in methanol and the solvent was removed under vacuum to afford 8.57 g (96%) of the title compound as an off-white foam. 1H NMR (200 MHz, CD3OD): δ 1.40 (s, 6H), 1.90 (m, 1H), 2.20-2.65 (m, 3H), 4.02 (s, 2H), 4.32 (m, 1H), 4.96 (d, 16 Hz, 1H), 5.00 (s, 2H), 5.25(d, 16 Hz, 1H), 7.08-7.65 (m, 17H). FAB-MS: calculated for C36H38N4 O4 590; found 591(M+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05672596 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-8db95db80d804e7d80cc251b5fb2d7d9 |
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| Source note | uspto-grants-1997_09 |
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