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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895794Generated: October 30, 2026

Sodium Iodide → HCID 10282284, compound

https://huagongshe.com/reaction/895794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant(3S,6S,7R,8R)-3-[[(3-Hydroxy-4-methoxy-2-pyridinyl)carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-methylpropanoateHCID 468590—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductHCID 10282284HCID 1028228481.4%

Reaction Steps

Benzyl bromide (0.233 mol, 27.7 mL) was added to a solution of NaI (0.097 mol, 14.5 g) in acetone (1 L). Natural product UK-2A (1) (0.194 mol, 100 g) was added followed by powdered K2CO3 (0.388 mol, 53 g) and the mixture stirred vigorously overnight. The mixture was diluted with CH2Cl2 (500 mL) and washed with H2O (2×500 mL). The organic layer was dried (MgSO4), and concentrated in vacuo. Recrystallization (EtOAc/hexane) gave 95.5 g (79%) of 2 as an off-white solid (m.p. 169-170° C.) which contained ˜6.5% N-benzylated product (LC-MS). 1H-NMR and MS (M+1 605) were consistent for the title compound (2). The compound was used in the next step without further purification. The N-benzylated by-product could be removed from the mixture prior to recrystallization by filtration of the crude reside through a plug of silica gel (30% acetone/hexane as the eluent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916932B2
Source datasetuspto-grants-2005_07
ORD IDord-c8eb4abe5cf34cc28168619f147843dd
Source noteuspto-grants-2005_07