Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379852Generated: November 1, 2026

Hydrochloric Acid → HCID 131720218, compound

https://huagongshe.com/reaction/1379852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 22877438HCID 22877438—
SolventMethanolHCID 887—
ProductHCID 131720218HCID 13172021896%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05672596
Source datasetuspto-grants-1997_09
ORD IDord-8db95db80d804e7d80cc251b5fb2d7d9
Source noteuspto-grants-1997_09