HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 11238729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 69313304 | HCID 69313304 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11238729 | HCID 11238729 | — |
Reaction Steps
Add 4M HCl/dioxane solution (400 μL, 1.60 mmol) to a solution of [2,3-dihydroxy-3-(4-nitro-phenyl)-propyl]-[2-(7-phenyl-isoquinoline-5-sulfonylamino)-ethyl]-carbamic acid tert-butyl ester (100 mg, 0.16 mmol in CH2Cl2 (3 mL) and CH3OH (2 mL) at room temperature under argon, and stir the mixture for 2 hours. Evaporate the solvent and wash the salt several times with Et2O and dry, to obtain the title compound. 1H NMR (CD3OD): δ9.95 (bs, 1H), 8.94-9.12 (m, 3H), 8.78 (m, 1H), 8.24 (m, 2H), 7.94 (m, 2H), 7.52-7.72 (m, 5H); 4.82-4.97 (m, 1H, under H2O signal), 4.07-4.15 (m, 1H), 3.05-3.31 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449477B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-e7c917fc96b148f497f69074440a4a57 |
| Source note | uspto-grants-2008_11 |