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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411295Generated: October 31, 2026

Sodium borohydride → HCID 90449966, compound

https://huagongshe.com/reaction/1411295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 90449869HCID 90449869—
SolventMethanolHCID 887—
ProductHCID 90449966HCID 9044996699%

Reaction Steps

The 1′-acetyl-N-(5-chlorothiazol-2-yl)-5-formylspiro[indoline-3,3′-pyrrolidine]-1-carboxamide (30.6 mg, 0.076 mmol) obtained in Step 2 of Example 401 was dissolved in methanol (1 mL). Thereafter, sodium borohydride (3.0 mg, 0.091 mmol) was added to the above obtained solution under cooling on ice, and the thus obtained mixture was then stirred at room temperature for 1 hour. Thereafter, the reaction solution was concentrated in vacuo, and the obtained residue was then purified by silica gel column chromatography (chloroform:methanol=10:1) to obtain the captioned compound (30.4 mg, 99%) in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-822974a0d136409db4f5f4e330b4528d
Source noteuspto-grants-2014_12