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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297096Generated: November 1, 2026

Triethylamine → HCID 136401067, compound

https://huagongshe.com/reaction/2297096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 136401068HCID 136401068—
SolventDimethylformamideHCID 6228—
ProductHCID 136401067HCID 13640106789%

Reaction Steps

Methyl 3-[1-[2-amino-4-oxopyrimidin-6-ylmethyl]-indazol-5-yl-carbonylamino]-2(S) -(1-naphthalenesulfonylamino)propionate. A mixture of the product prepared according to Example E-24 Part F (85 mg, 298 μmol) and the product prepared according to Example E-24 Part H (113 mg, 328 μmol) in N,N-dimethylformamide (3 mL) was treated sequentially with triethylamine (52 μL, 373 μmol), 1-hydroxybenzotriazole hydrate (40 mg, 298 μmol) and dicyclohexylcarbodiimide (68 mg, 328 μmol). The mixture was stirred at room temperature for 24 h and concentrated. The residue was purified by flash chromatography (dichloromethane-methanol, 97:3 then 9:1) to provide the title product (154 mg, 89%) as a gum: 1H NMR (MeOH-d4) d 8.64 (d, 1H), 8.15 (s, 2H), 7.92 (d, 1H), 7.89 (s, 1H), 7.71 (d, 1H), 7.6-7.3 (4H), 5.35 (s, 2H), 5.03 (s, 1H), 4.20 (dd, 1H), 3.64 (dd, 1H), 3.46 (dd, 1H); ester methyl signal obscured by residual MeOH signal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489333B2
Source datasetuspto-grants-2002_12
ORD IDord-030d379f7a2944898c649c7b149a93ca
Source noteuspto-grants-2002_12