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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244363Generated: November 2, 2026

2-Methylbenzoyl chloride → [2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,7,8-tetrahydro-1H-imidazo[4,5-d]azepin-6-yl]-o-tolyl-methanone

https://huagongshe.com/reaction/1244363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzoyl chlorideHCID 70276—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-Methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-1,4,5,6,7,8-hexahydro-imidazo[4,5-d]azepine hydrochlorideHCID 11441590—
SolventTetrahydrofuranHCID 8028—
Product[2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,7,8-tetrahydro-1H-imidazo[4,5-d]azepin-6-yl]-o-tolyl-methanoneHCID 1178538698.4%

Reaction Steps

To a suspension of 0.04 g 2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-1,4,5,6,7,8-hexahydro-imidazo[4,5-d]azepine hydrochloride in 3.4 ml tetrahydrofurane were added at 0–4° C. 0.07 ml N-ethyldiisopropylamine and 0.017 g o-toluoyl chloride. The mixture was refluxed for 17 hours, silicagel was added and the solvent was distilled off. The residue was transferred to a column prefilled with silicagel and was chromatographed with dichloromethane/methanol 96:4 to yield 0.047 g (94%) [2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,7,8-tetrahydro-1H-imidazo[4,5-d]azepin-6-yl]-o-tolyl-methanone as yellow solid; M.p.: 194–196° C.; MS (ISP): m/e=504 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-b2b58a23e54446d39b44be9347b148f6
Source noteuspto-grants-2006_10