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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680013Generated: October 29, 2026

Hydrochloric Acid → HCID 23458748, compound

https://huagongshe.com/reaction/1680013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 23458739HCID 23458739—
SolventDimethylformamideHCID 6228—
ProductHCID 23458748HCID 2345874886.7%

Reaction Steps

18.6 g (0.03 mole) of tert-butyl 4-benzyloxycarbonyl-8-phenyl-alpha-phthalimido-1-thia-3,8-diazaspiro[4.5]decane-2-acetate (obtained in 3.3) are suspended in 50 ml of N,N'-dimethylformamide. A solution containing 2 g (0.04 mole) of hydrazine hydrate in 20 ml of N,N-dimethylformamide is added dropwise at 0° C. under an atmosphere of nitrogen. The reaction mixture is allowed to warm up to ambient temperature and stirred for 1 hour. The reaction mixture is then again cooled to 0° C. and slowly neutralized by the addition of 33.75 ml of 1N hydrochloric acid, whereafter it is stirred at ambient temperature for 2 hours after which time it solidifies. 300 ml of water are added, followed by extraction with chloroform. The organic phase is washed with water, dried with anhydrous sodium sulfate and evaporated to dryness. The residue is triturated with diethyl ether, filtered and the precipitate washed with diethyl ether. There are obtained 12.8 g of tert-butyl alpha-amino-4-benzyloxycarbonyl-8-phenyl-1 -thia-3,8-diazaspiro[4.5]decane-2-acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271172
Source datasetuspto-grants-1981_06
ORD IDord-84f2146a018a47dcb9001d097d4ce36b
Source noteuspto-grants-1981_06