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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600405Generated: October 30, 2026

Benzimidazole → HCID 86622937, compound

https://huagongshe.com/reaction/600405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantHCID 86622938HCID 86622938—
ProductHCID 86622937HCID 8662293746%

Reaction Steps

Pale yellow solid. 46% yield on 2 steps (reduction and benzimidazole closing), on 2.47 mmol scale. Synthesized from 2-(2-amino-5-chlorophenylamino)-6-chloro-9-(tetrahydro-2H-pyran-4-yl)-7H-purin-8(9H)-one. 1H NMR (300 MHz, CDCl3+CD3OD) δ, ppm: 9.08 (s, 1H), 8.61 (s, 1H), 7.74 (d, 1H), 7.40 (d, 1H), 4.65-4.58 (m, 1H), 4.23-4.19 (m, 2H), 3.62 (appt, 2H), 2.82-2.76 (m, 2H), 1.93 (br d, 2H); MS (EI) m/z 405.2 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902187B2
Source datasetuspto-grants-2011_03
ORD IDord-bb1114ccc6f049ebbdb652262c3493fc
Source noteuspto-grants-2011_03