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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660322Generated: November 2, 2026

Hydrochloric Acid → HCID 15575766, compound

https://huagongshe.com/reaction/1660322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
ReactantSodiumHCID 5360545—
ReactantHCID 13278825HCID 13278825—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 15575766HCID 1557576643.1%

Reaction Steps

4-(2-tert.-Butoxycarbonylamino-ethyl)-thiosemicarbazide (9.37 g) is added to a solution of sodium (0.92 g) in methanol (40 cc) at 20° C., and diethyl oxalate (5.4 g) is then introduced dropwise in the course of 10 minutes. The mixture is heated under reflux for 3 hours. It is allowed to cool, water (100 cc) is added, concentrated hydrochloric acid (3 cc) is introduced dropwise, the mixture is extracted with ethyl acetate (2×100 cc) and the extract is washed with a saturated sodium chloride solution (2×50 cc), dried ocer sodium sulphate, filtered and concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa). The residue is taken up in methylene chloride (65 cc), the crystallisation is started, the batch is left for 2 hours at 20° C. and then filtered, and white crystals (4.59 g) of 4-(2-tert.-butoxycarbonylamino-ethyl)-5,6-dioxo-3-thioxoperhydro-1,2,4-triazine, melting at 160° C., are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307116
Source datasetuspto-grants-1981_12
ORD IDord-fe515f2f653246859a352da497d480d7
Source noteuspto-grants-1981_12