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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358461Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 68675033, compound

https://huagongshe.com/reaction/2358461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantOxalyl chlorideHCID 65578—
Reactant1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acidHCID 68674009—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 68675033HCID 68675033—

Reaction Steps

To a suspension of 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid (as prepared in Example 16; (2.0 g, 6.8 mmol) in dichloromethane (60 ml) was added oxalyl chloride (1.2 ml, 14 mmol) and the reaction stirred for 2 h and left to stand overnight. The solvent and excess reagent was removed in vacuo. The resulting residue was dissolved in dichloromethane (10 ml) and added dropwise to a cooled solution (ice/methanol bath) of hydrazine hydrate (1.7 ml, 34 mmol) in diethyl ether (60 ml) over 5 mins. The reaction mixture was then stirred for a further 40 mins before being reduced to half its volume in vacuo and filtered. The filtrate was concentrated further and the resulting precipitate filtered. The precipitates were combined and dried in vacuo to afford 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid hydrazide (2.3 g, 7 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763732B2
Source datasetuspto-grants-2010_07
ORD IDord-4b506a30b1644b17aeef5caa0a6afbff
Source noteuspto-grants-2010_07