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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294857Generated: November 1, 2026

Methanol → HCID 21471820, compound

https://huagongshe.com/reaction/2294857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalateHCID 71081—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21471929HCID 21471929—
ProductHCID 21471820HCID 21471820—

Reaction Steps

To a solution of 0.4 g of 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)acetyl)-2-methyl-5,6,7,8-tetrahydro-4H-thieno[3,2-c]azepin-4-one (m.p. 175°-176° C. as oxalate thereof) in 20 ml of methanol was added 0.5 g of sodium borohydride under cooling. The mixture was stirred for 10 minutes and concentrated. Water was added thereto and the solution was extracted with ethyl acetate. The extract was washed with water, dried and the solvent was distilled away. The residue was treated with fumaric acid in ethanol and recrystallized from ethanol to give 0.22 g of 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)-1-hydroxyethyl)-2-methyl-5,6,7,8-tetrahydro-4H-thieno[3,2-c]azepin-4-one difumarate monohydrate, m.p. 116°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691330
Source datasetuspto-grants-1997_11
ORD IDord-608ca74468fc4d17b7aa3adc3e0bb067
Source noteuspto-grants-1997_11