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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374862Generated: November 2, 2026

Methanol → HCID 21076923, compound

https://huagongshe.com/reaction/1374862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 69021338HCID 69021338—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21076923HCID 21076923100.1%

Reaction Steps

To a solution of 1-benzyl-2-{(R)-[(3-tert-butoxycarbonylamino-propyl)-(1-p-tolyl-methanoyl)-amino]-methyl-propyl}-4-methyl-6-oxo-1,6-dihydro-pyrimdine-5-carboxylic acid methyl ester (2.75 g, 4.55 mmol) in THF (60 mL) was added MeOH (30 mL) followed by 1N KOH (18.2 mL, 18.2 mmol). The resultant solution was heated to 60° C. for 3 h, then concentrated under reduced pressure. The residue was diluted with H2O (75 mL), adjusted to pH˜7 with 1N HCl, and extracted with EtOAc (3×75 mL). The extracts were dried over Na2SO4, filtered and concentrated under reduced pressure to give 2.69 g (100%) of 1-benzyl-2-{(R)-[(3-tert-butoxycarbonylamino-propyl)-(1-p-tolyl-methanoyl)-amino]-methyl-propyl}-4-methyl-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid as an oil which was used in the subsequent step without purification: MS (ES) m/e 591.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166595B2
Source datasetuspto-grants-2007_01
ORD IDord-2e397ea17ff345639b638d260e5732dd
Source noteuspto-grants-2007_01