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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268933Generated: November 1, 2026

Acetic Acid → Merck SIP Agonist

https://huagongshe.com/reaction/1268933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-azetidinecarboxylic AcidHCID 93192—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant[4-[5-[4-(2-Methylpropyl)phenyl]-1,2,4-oxadiazol-3-yl]phenyl]methanolHCID 11645224—
SolventMethanolHCID 887—
ProductMerck SIP AgonistHCID 1043054974%

Reaction Steps

A solution of 3.06 g (10.0 mmol) of Aldehyde 1, 1.06 g (10.5 mmol) of 3-azetidine carboxylic acid and 5 mL of acetic acid in 150 mL of methanol was stirred for 20 min at rt. A solution of sodium cyanoborohydride (380 mg, 5.0 mmol) in 20 mL of methanol was added. The reaction mixture was stirred for 1 h then was filtered. The solids were washed with 30 ml of methanol and dried to afford 2.88 g (74%) of the title compound: 1H NMR (400 Mhz, CD3OD) δ 0.95 (d, J=6.6, 6H), 1.96 (m, 1H), 2.62 (d, J=7.3, 2H), 3.42 (m, 1H), 4.19 (m, 4H), 4.41 (s, 2H), 7.43 (d, J=8.0, 2H), 7.64 (d, J=8.2, 2H), 8.14 (d, J=8.0, 2H), 8.23 (d, J=8.2, 2H); ESI-MS 392 (M+H); LC-1: 3.0 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199142B2
Source datasetuspto-grants-2007_04
ORD IDord-fbe47b1e6b884ac697340a2fc5989673
Source noteuspto-grants-2007_04