1988
DOI: 10.1002/chin.198847170
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ChemInform Abstract: Reaction of N‐Alkyl/Aralkylisatoic Anhydrides with Aroylhydrazines: Formation of 1,3,4‐Oxadiazoles and 1,4‐Dihydro‐5H‐1,3,4‐benzotriazepin‐5‐one.

Abstract: The reaction of the anhydrides (I) with aroylhydrazines such as (II) under the conditions shown gives products of type (III).

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“…M.p. 188–192°C as reported (Ibrahim, Abo‐Kul, Soltan, Barkat, & Helal, ; Reddy, Reddy, & Ratnam, ; Reddy & Reddy, ). 1 H NMR (DMSO, d 6 ) δ 2.80 (3H, d, J = 4.9, NCH 3 ), 6.61 (1H, t, J = 7.4, ph H), 6.69 (1H, d, J = 8.4, ph H), 7.36 (1H, t, J = 7.7, ph H), 7.51–7.60 (4H, m, ph H + NH), 7.68 (1H, d, J = 6.9, ph H), 7.93 (2H, d, J = 7.2, ph H), 10.24 (1H, s, NHCO), 10.39 (1H, s, NHCO).…”
Section: Methodssupporting
confidence: 75%
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“…M.p. 188–192°C as reported (Ibrahim, Abo‐Kul, Soltan, Barkat, & Helal, ; Reddy, Reddy, & Ratnam, ; Reddy & Reddy, ). 1 H NMR (DMSO, d 6 ) δ 2.80 (3H, d, J = 4.9, NCH 3 ), 6.61 (1H, t, J = 7.4, ph H), 6.69 (1H, d, J = 8.4, ph H), 7.36 (1H, t, J = 7.7, ph H), 7.51–7.60 (4H, m, ph H + NH), 7.68 (1H, d, J = 6.9, ph H), 7.93 (2H, d, J = 7.2, ph H), 10.24 (1H, s, NHCO), 10.39 (1H, s, NHCO).…”
Section: Methodssupporting
confidence: 75%
“…M.p. 176–178°C as reported (Reddy et al, ; Reddy & Reddy, ). 1 H NMR (DMSO, d 6 ) δ 2.78 (3H, d, J = 5, NCH 3 ), 3.53 (2H, s, CH 2 CO), 6.56 (1H, t, J = 7.5, ph H), 6.66 (1H, d, J = 8.3, ph H), 7.24–7.34 (6H, m, ph H + NH), 7.48 (1H, d, J = 4.7, ph H), 7.58 (1H, d, J = 6.8, ph H), 10.05 (1H, s, NHCO), 10.08 (1H, s, NHCO).…”
Section: Methodssupporting
confidence: 72%
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