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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid | HCID 68674009 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68675033 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763732B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-4b506a30b1644b17aeef5caa0a6afbff |
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| Source note | uspto-grants-2010_07 |
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