HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844967Generated: October 31, 2026
Isoquinoline-3-carboxaldehyde → HCID 58026348, compound
https://huagongshe.com/reaction/1844967
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoquinoline-3-carboxaldehyde | HCID 231555 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178508178 | HCID 178508178 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 58026348 | HCID 58026348 | 7.3% |
Reaction Steps
To a solution of 150 mg (0.95 mmol) of isoquinoline-3-carbaldehyde in dry DCE (1 mL) was added 60 mg (0.25 mmol) of 2-amino-3H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide (intermediate B), and Ti(OiPr)4 (3 mL). The mixture was sonciated for 30 min then stirred at room temperature for 6 h. NaBH4 (0.5 g) was added, and the mixture was stirring for 12 h. The reaction was quenched by addition of methanol (2 mL). After usual workup, the residue was purified by column chromatography eluting with DCM then EtOAc/methanol (v/v=100:5) to give 7 mg (7%) of 2-[(isoquinolin-3-ylmethyl)-amino]-1H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide. LCMS: 384 (M+1)+. 1H NMR (DMSO-d6, 400 MHz): δ 12.58 (s, 1H), 11.8 (s, 1H), 11.6 (s, 1H), 9.07 (s, 1H), 8.69 (s, 1H), 8.22 (t, 1H), 7.96 (d, 1H), 7.91 (d, 1H), 7.67 (m, 2H), 7.53 (t, 1H), 7.36 (d, 1H), 7.02 (t, 1H), 6.90 (s, 1H), 6.85 (s, 1H), 4.78 (d, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946259B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-60344591a7154eba87898146990d71b3 |
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| Source note | uspto-grants-2015_02 |
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