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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086284Generated: October 31, 2026

HCID 131716928, compound → HCID 131716927, compound

https://huagongshe.com/reaction/1086284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131716928HCID 131716928—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 131716927HCID 13171692759%

Reaction Steps

0.63 g of 1-[3-(5-nitroindan-2-ylacetyl)-L-thioprolyl]pyrrolidine prepared in Example 29 was dissolved in a mixed solution of 9 ml of acetic acid and 6 ml of water. 1.00 g of iron powder was gradually added with stirring. After 1 hour, the iron powder was filtered. The filtrate was alkalinized using 10% sodium hydroxide and extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. After evaporating the solvent, the residue obtained was purified by silica gel chromatography to produce 0.34 g of 1-[3-(5-aminoindan-2-ylacetyl)-L-thioprolyl]pyrrolidine as a brownish and oily substance (yield: 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028604
Source datasetuspto-grants-1991_07
ORD IDord-803c0d9c015643f89a47e7d404156e8b
Source noteuspto-grants-1991_07