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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804556Generated: November 1, 2026

Acetohydrazide → HCID 57637130, compound

https://huagongshe.com/reaction/1804556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductHCID 57637130HCID 57637130—

Reaction Steps

25.00 g (132 mmol) 3-tert-butoxycarbonylamino-propionic acid, 11.45 g (130 mmol) ethanoic acid hydrazide, 50.91 g (159 mmol) O-(1H-benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) and 50 ml diisopropylethylamine are stirred in 500 ml of tetrahydrofuran/dichloromethane for 24 hours at ambient temperature. Then the mixture is evaporated down, the residue is extracted with ethyl acetate and 10% potassium hydrogen carbonate solution. The organic phase is dried and evaporated to dryness. The residue is crystallised from isopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354418B2
Source datasetuspto-grants-2013_01
ORD IDord-178f1cf8d6bb43d8b6ec67fa9e3b3455
Source noteuspto-grants-2013_01