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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431511Generated: November 3, 2026

1,4,5,6-Tetrahydropyrimidin-2-amine → (2s)-2-(1-Adamantylmethoxycarbonylamino)-3-((5-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-cyclopropyl)-thiophene-2-carbonyl)-amino)-propionic acid tert-butyl ester

https://huagongshe.com/reaction/431511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4,5,6-Tetrahydropyrimidin-2-amineHCID 3287412—
Reactant2-(5-(((2s)-2-(1-Adamantylmethoxycarbonylamino)-2-tert-butoxycarbonyl-ethyl)carbamoyl)-2-thienyl)-cyclopropancarboxylic acid methyl esterHCID 57248699—
SolventDimethylformamideHCID 6228—
Product(2s)-2-(1-Adamantylmethoxycarbonylamino)-3-((5-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-cyclopropyl)-thiophene-2-carbonyl)-amino)-propionic acid tert-butyl esterHCID 69637307—

Reaction Steps

The product obtained in step b) was dissolved in 4 ml of anhydrous dimethylformamide and stirred under an argon atmosphere with 99 mg of 2-amino-1,4,5,6-tetrahydropyrimidine for 7 hours at room temperature. The solvent was removed in vacuo and the residue was chromatographed (silica gel; ethyl acetate/methanol (1/1, v/v)). The fractions containing the title compound were pooled and evaporated under reduced pressure to give 53 mg of a colourless resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660728B2
Source datasetuspto-grants-2003_12
ORD IDord-9152ad8f8b2647a3a50b0fda14815517
Source noteuspto-grants-2003_12