HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850368Generated: October 31, 2026
Sodium borohydride → HCID 70291348, compound
https://huagongshe.com/reaction/850368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70289412 | HCID 70289412 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70291348 | HCID 70291348 | 108.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017929 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-78b2146dae3e42efb86e5aab08fb88af |
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| Source note | uspto-grants-2000_01 |
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