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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854249Generated: October 30, 2026

(2S)-2-benzyloxycarbonylamino-3-{9-[3-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-propyl]-9H-purin-6-ylamino}-propionic acid tert-butyl ester → (2S)-2-Benzyloxycarbonylamino-3-{9-[3-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-propyl]-9H-purin-6-ylamino}-propionic Acid

https://huagongshe.com/reaction/854249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-benzyloxycarbonylamino-3-{9-[3-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-propyl]-9H-purin-6-ylamino}-propionic acid tert-butyl esterHCID 15547266—
SolventTrifluoroacetic acid waterHCID 22392675—
Product(2S)-2-Benzyloxycarbonylamino-3-{9-[3-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-propyl]-9H-purin-6-ylamino}-propionic AcidHCID 15547257—

Reaction Steps

70 mg (Q.12 mmol) of (2S)-2-benzyloxycarbonylamino-3-{9-[3-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-propyl]-9H-purin-6-ylamino}-propionic acid tert-butyl ester was dissolved in 3 ml of trifluoroacetic acid/water (95/5). The solution was stirred at room temperature for 3 hours. The solvent was removed in vacuo and toluene was added to the residue and then removed in vacuo. The residue was dissolved in acetonitrile/water 1/1 and lyophilized. Yield: 51 mg (trifluoroacetate salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259159B2
Source datasetuspto-grants-2007_08
ORD IDord-35830b427dad41b291ce0bbbf227bea8
Source noteuspto-grants-2007_08