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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850368Generated: October 31, 2026

Sodium borohydride → HCID 70291348, compound

https://huagongshe.com/reaction/850368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70289412HCID 70289412—
SolventMethanolHCID 887—
ProductHCID 70291348HCID 70291348108.4%

Reaction Steps

Dissolved in 20 ml of methanol were 500 mg of 3-(1-oxo-2-indanacetyl)-4-(R)-(1-pyrrolidinecarbonyl) thiazolidine, and 80 mg of NaBH4 were added to the solution. After stirring the mixture at room temperature, the resultant liquid reaction mixture was concentrated under reduced pressure, and the residue was added with water and extracted with chloroform. After the extract was dried over anhydrous magnesium sulfate, chloroform was distilled off under reduced pressure to obtain 545 mg of 3-(1-hydroxy-2-indanacetyl)-4-(R)-(1-pyrrolidinecarbonyl)thiazolidine. Thereafter, the process was allowed to progress in accordance with the process of Synthetic Example 1, thereby obtaining the title compound as a diastereomeric mixture. Yield: 87% (amorphous).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017929
Source datasetuspto-grants-2000_01
ORD IDord-78b2146dae3e42efb86e5aab08fb88af
Source noteuspto-grants-2000_01