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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282021Generated: October 29, 2026

Tris(hydroxymethyl)aminomethane → HCID 12043808, compound

https://huagongshe.com/reaction/1282021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 3780288HCID 3780288—
Reactanttert-butyl 5-amino-3-cyclopropyl-1H-pyrazole-1-carboxylateHCID 11356513—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 12043808HCID 1204380870%

Reaction Steps

265 mg (1 mmol) of 2-{4-[(tert-butoxycarbonyl)amino]phenyl}propanoic acid were treated at 4° C. under nitrogen with 146 μl (2 mmol) of thionylchloride. The reaction mixture was stirred for 2.5 hours and the temperature was gradually raised to room temperature. The mixture was taken up with tetrahydrofuran and evaporated thoroughly. The resulting acyl chloride, without any further purification, was dissolved in 3 ml of dry tetrahydrofuran and added dropwise to a solution of 178 mg (0.8 mmol) of tert-butyl-5-amino-3-cyclopropyl-1H-pyrazole-1-carboxylate in 3 ml of tetrahydrofuran. 312 mg (1 mmol, loading 3.2 mmol/g) of polymer supported triethylamine were then added under stirring. After 2.5 hours 80 mg (loading 3.2 mmol/g) of polymer supported trisamine were finally added in order to quench the excess of acyl chloride. After 2 hours, the resins were filtered and washed with methanol and dichloromethane. Evaporation of the filtrate afforded 263 mg of the title compound as a foam (70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455559B1
Source datasetuspto-grants-2002_09
ORD IDord-abb4b32e56e847f086e76a7364723d08
Source noteuspto-grants-2002_09