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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332928Generated: October 29, 2026

Potassium Hydroxide → (S)-2-amino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid amide

https://huagongshe.com/reaction/332928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(S)-2-tert-butoxycarbonylamino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid amideHCID 56832948—
SolventHydrochloric AcidHCID 313—
Product(S)-2-amino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid amideHCID 56832949100.9%

Reaction Conditions

Temperature5 °C

Reaction Steps

(S)-2-tert-Butoxycarbonylamino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid amide (48.5 g, 136 mmol, >99.9% ee) is introduced at 40° C. in portions into hydrochloric acid (16% strength, 80 ml), and the resulting solution is stirred for 1 h at this temperature. After cooling to 5° C., the pH is adjUsted to 10 by adding concentrated potassium hydroxide solution. The precipitated solid is filtered off with suction and dried to give (S)-2-amino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid amide (35.3 g, 80% yield, 79% content, 99.8% ee) as a colorless solid, which can be further reacted or else crystallized again from aqueoUs solution, as desired.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877926B2
Source datasetuspto-grants-2014_11
ORD IDord-7468ad6c8bcd42888a6707c1e4755f38
Source noteuspto-grants-2014_11