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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768030Generated: October 31, 2026

Sodium triacetoxyborohydride → HCID 11407042, compound

https://huagongshe.com/reaction/1768030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 23614432HCID 23614432—
Reactant1-(7-Methoxy-1-benzofuran-3-yl)propan-2-oneHCID 23614434—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
ProductHCID 11407042HCID 11407042—

Reaction Steps

3-{1-[2-(7-methoxy-1-benzofuran-3-yl)-1-methylethyl]-1,2,3,6-tetrahydro-4-pyridinyl}-6-fluoro-1H-indole was prepared by generally following the procedure outlined in example 41, step 2, starting from the 1-(7-methoxy-1-benzofuran-3-yl)acetone (204 mg, 1 mmol) and 3 (1,2,3,6-tetrahydro-4-pyridinyl)-6-fluoro-1H-indole (216.0 mg, 1 mmol) in 1,2-dichloroethane (100 ml) and acetic acid (1 ml), sodium triacetoxyborohydride (422 mg, 2 mmol). The product was purified by silica-gel column chromatography by eluting it with 80% ethyl acetate:hexane. Brown solid; Yield: 60 mg (14%); 405 (M+H); 1HNMR (400 MHz, CDCl3): δ 8.31 (broad, s, 1H, NH); 7.92˜6.88 (m, 7H); 6.25 (s, 1H); 3.85 (s, 3H), 3.50˜2.60 (m, 10H); 1.03˜1.05 (d, J=8.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-9669c439cfcb400c80e2aa745d1519ae
Source noteuspto-grants-2007_06