HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481935Generated: October 31, 2026
Hydrochloric Acid → HCID 118677395, compound
https://huagongshe.com/reaction/1481935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 118677378 | HCID 118677378 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 118677395 | HCID 118677395 | 78.69% |
Reaction Steps
To a solution of tert-butyl N-[(1S)-2-[[(3S)-5-[4-[(3S)-3-[[(2S)-2-[tert-butoxycarbonyl(methyl)amino]propanoyl]amino]-7-cyano-1-[(2-methyl-1-naphthyl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepine-5-carbonyl]benzoyl]-7-cyano-1-[(2-methyl-1-naphthyl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]amino]-1-methyl-2-oxo-ethyl]-N-methyl-carbamate (27 mg, 0.022 mmol) in dioxane (3 mL) at 0° C. was added 4 M HCl in dioxane (2 mL). The mixture was stirred at 0° C. for 10 min, and the cooling bath was removed. After 16 h, the mixture was concentrated and the residue was triturated with diethyl ether to afford the title compound as a white solid (19 mg, 78.69%). LC-MS: 1013.8 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409888B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-8edb08cae1024ba1b0c386f1bcbb7611 |
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| Source note | uspto-grants-2016_08 |
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