Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415612Generated: November 2, 2026

Tetrahydrofuran → HCID 178477880, compound

https://huagongshe.com/reaction/2415612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCyano-borohydrideHCID 498716—
Reactant1H-Indole-6-carboxaldehydeHCID 2773435—
ReactantHCID 178511631HCID 178511631—
SolventAcetic AcidHCID 176—
ProductHCID 178477880HCID 178477880—

Reaction Steps

A mixture of example 23A (30 mg, 0.11 mmol), 6-formylindole (19.2 mg, 0.132 mmol) and solid supported cyanoborohydride (0.22 mmol) was shaken in 1:1 mixture tetrahydrofuran and acetic acid for 15 hours, filtered and concentrated. The residue was purified with a high throughput HPLC system to provide the desired compound as its bis TRIFLUOROACETIC ACID salt. MS (ESI(+)Q1MS m/z 405 (M+H)+); 1H NMR (300 MHz, DMSO-D6) δ ppm 11.31 (s, 1 H), 8.74 (d, 1 H), 8.49-8.79 (m, 2 H), 7.96 (d, 1 H), 7.85 (dd, 1 H), 7.62 (d, 1 H), 7.56 (s, 1 H), 7.45 (t, 1 H), 7.13 (d, 1 H), 6.94 (d, 1 H), 6.47 (t, 1 H), 4.28 (br.s, 1 H), 4.08 (br.s, 1 H), 2.27 (s, 2 H), 1.73-2.13 (m, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818772B2
Source datasetuspto-grants-2004_11
ORD IDord-c7ba6c65f5444e4ca9867dc7c0ed770e
Source noteuspto-grants-2004_11