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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729320Generated: October 30, 2026

2-Aminobenzimidazole → 4-(1H-Benzimidazol-2-ylamino)-2-butyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide

https://huagongshe.com/reaction/729320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzimidazoleHCID 13624—
Reactant2-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 67242623—
Product4-(1H-Benzimidazol-2-ylamino)-2-butyl-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 11632646—

Reaction Steps

The title compound was prepared from 2-butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide and 2-amino-1H-benzimidazole in a similar manner as described for e.g. Examples 6-9, 22-25, 28 and 32-35. 1H NMR (500 MHz, CD3CN): δ 1.00 (t, 3H), 1.43-1.53 (m, 2H), 1.76-1.85 (m, 2H), 3.71 (t, 2H), 7.12-7.19 (m, 4H), 7.34-7.68 (m, 5H), 8.03-8.06 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582629B2
Source datasetuspto-grants-2009_09
ORD IDord-85dbe2f8367b4828b1fd582533ad3db3
Source noteuspto-grants-2009_09