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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666310Generated: October 29, 2026

Sodium borohydride → HCID 67081706, compound

https://huagongshe.com/reaction/1666310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67081860HCID 67081860—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 67081706HCID 6708170672.1%

Reaction Steps

A solution of 2-methyl-4-(3,5-dimethoxyphenyl)-4-(phenylsulfanyl)-7-methoxy-1,4-dihydro-3(2H)-isoquinolone (2.4 g) and nickel chloride hexahydrate (8.8 g) in methanol-tetrahydro-furan (3:1, 100 ml) was cooled to 0° C. Sodium borohydride (4.2 g) was added in small portions during 30 minutes at a temperature not exceeding 5° C. The slurry was filtered and the filtrate concentrated to dryness. The residue was partitioned between dichloromethane (200 ml) and aqueous sodium hydroxide (2M, 200 ml). The organic phase was dried and concentrated to dryness leaving crude 2-methyl-4-(3,5-dimethoxyphenyl)-7-methoxy-1,4-dihydro-3(2H)-isoquinolinone (1.3 g). Crystallization from methanol afforded the pure compound, m.p. 137-139

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044067B2
Source datasetuspto-grants-2011_10
ORD IDord-c84cf7c4af9d4c568e4a4dacdc0634ce
Source noteuspto-grants-2011_10