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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755434Generated: October 29, 2026

Ammonia → tert-Butyl 2-thioureidoacetate

https://huagongshe.com/reaction/1755434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantGlycine tert-butyl esterHCID 151417—
Reactant1,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 853162—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-thioureidoacetateHCID 57225720—

Reaction Steps

To a magnetically stirred suspension of tert-butyl 2-aminoacetate (11.2 g, 85 mmol) in CH2Cl2 (200 mL) under nitrogen is added 1,1′-thiocarbonyldipyridin-2(1H)-one (21 g, 90 mmol) and the resulting mixture is stirred at room temp. for 18 h. The solvent is removed in vacuo, the residue treated with 2M ammonia in methanol (600 mL, 1200 mmol) and stirred at room temperature for 45 min. The solvent is removed in vacuo and dried under high vacuum to give the title compound as a reddish oil that is used “as is” without further purification in the next step. LC/MS (Condition A): ret. T=2.19 min, (M+H)+ 191—actually see (M−55) 134.95 (this is characteristic of BOC fragmentation pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169295B2
Source datasetuspto-grants-2015_10
ORD IDord-3a4a769d4f4a40a2b6a52cf533babe2d
Source noteuspto-grants-2015_10