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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844967Generated: October 31, 2026

Isoquinoline-3-carboxaldehyde → HCID 58026348, compound

https://huagongshe.com/reaction/1844967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinoline-3-carboxaldehydeHCID 231555—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178508178HCID 178508178—
CatalystHCID 178460666HCID 178460666—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58026348HCID 580263487.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946259B2
Source datasetuspto-grants-2015_02
ORD IDord-60344591a7154eba87898146990d71b3
Source noteuspto-grants-2015_02