Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481258Generated: November 3, 2026

Hydrochloric Acid → (6S,8S)-3-{[(Benzyloxy)carbonyl][3-(trifluoromethyl)benzyl]amino}-8-[2-(benzyloxy)-2-oxoethyl]-8-methyl-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylic acid

https://huagongshe.com/reaction/481258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantLithium HydroxideHCID 3939—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 86587578HCID 86587578—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(6S,8S)-3-{[(Benzyloxy)carbonyl][3-(trifluoromethyl)benzyl]amino}-8-[2-(benzyloxy)-2-oxoethyl]-8-methyl-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylic acidHCID 69974009124.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 117d (537 mg, 0.651 mmol) in 4:1 THF/H20 at 0° C., were added 30% H2O2 (0.295 mL, 2.604 mmol) and 1M LiOH (1.107 mL, 1.107 mmol). The mixture was stirred at 0° C. for 2 h, then a solution of Na2SO3 (140 mg, 1.107 mmol) in 1 mL H2O was added dropwise. The mixture was poured into 0.5 M HCl and the product was extracted with EtOAc. The organic was washed with brine, dried (Na2SO4), and concentrated to afford 527 mg of 117e, which was contaminated with BocNHPh. The mixture was used as is in the following step. MS(ESI) 650.3 (M+H+); 648.3 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653295B2
Source datasetuspto-grants-2003_11
ORD IDord-b0488b6c9d1841f0809c3836fc9e2b8a
Source noteuspto-grants-2003_11