HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 58840722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23585502 | HCID 23585502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58840722 | HCID 58840722 | — |
Reaction Steps
To a suspension of 4-amino-2-(6-oxo-5,6,7,8-tetrahydro-naphthalen-2-yl)-thieno[3,2-c]pyridine-7-carboxylic acid amide 89 (24.5 mg, 0.07 mmol) in absolute ethanol (4 mL) was added sodium borohydride (11.5 mg, 0.30 mmol). After 1.25 h at room temperature, the reaction mixture was concentrated, partially dissolved in a mixture of DMSO and MeOH, and filtered. The filtrate was purified by reverse phase preparative HPLC to give 90. 1H NMR (400 MHz, d6-DMSO) δ: 1.63-1.74 (m, 1H), 1.87-1.96 (m, 1H), 2.57-2.68 (m, 1H), 2.73-2.81 (m, 1H), 2.90-3.02 (m, 2H), 3.93-4.01 (m, 2H), 7.20 (d, J8.0 Hz, 1H), 7.44-7.48 (m, 2H), 7.70-7.83 (br s, 1H), 8.26 (s, 2H), 8.41 (s, 1H), 8.63-8.83 (br s, 2H). MS (EI) m/z (M+H+) 340, (2M+H+) 679.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07635695B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-ccfae9904b334aae839a4f5487f6a8cf |
| Source note | uspto-grants-2009_12 |