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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463909Generated: October 31, 2026

Ethanol → HCID 67809643, compound

https://huagongshe.com/reaction/1463909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67807695HCID 67807695—
SolventAcetic AcidHCID 176—
ProductHCID 67809643HCID 67809643123.5%

Reaction Steps

A solution of 0.2 g (0.25 mmol) of (E)-5-[2-[4-(2-chlorophenyl)-9-methyl-6H-thieno-[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl]ethyl]-2-[2-[3-[2-(4-cyclobutyl-2-thiazolyl)ethenyl]phenylamino]-2-oxoethyl]-benzoic acid ethyl ester, 4 mL of 1N NaOH, 11 mL of H2O, and 15 mL of ethanol was stirred for 40 hours and acidified with acetic acid. The product was extracted with CH2Cl2, which was dried and concentrated. The residue was chromatographed on silica gel using ethyl acetate/ethanol (10:1) followed by the same mixture (4:1) as the eluent. The fractions containing the product were concentrated and the residue triturated with ether/pet. ether and filtered to give 0.12 g (61%) of (E)-5-[2-[4-(2-chlorophenyl)-9-methyl-6H-thieno-[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl]ethyl]-2-[2-[3-[2-(4-cyclobutyl-2-thiazolyl)ethenyl]phenylamino]-2-oxoethyl]-benzoic acid monohydrate as an off-white powder: mp 143°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302590
Source datasetuspto-grants-1994_04
ORD IDord-5cc0a7a07d774c68871ee5d51e7a79d7
Source noteuspto-grants-1994_04