Phosphorus pentachloride → 2-chloro-6-fluoro-N-(4-iodophenyl)benzenecarbohydrazonoyl chloride

HRID 508715

反応式

HRID 508715 の反応式
[Cl:1][C:2]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[C:3]=1/[CH:4]=[N:5]/[NH:6][C:7]1[CH:12]=[CH:11][C:10]([I:13])=[CH:9][CH:8]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:20]>C1C=CC=CC=1>[Cl:1][C:2]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[C:3]=1[C:4]([Cl:20])=[N:5][NH:6][C:7]1[CH:8]=[CH:9][C:10]([I:13])=[CH:11][CH:12]=1

参加物

4

反応物 2

HCID 24819Phosphorus pentachlorideHCID 90020166N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]-4-iodoaniline

生成物 1

HCID 1317332342-chloro-6-fluoro-N-(4-iodophenyl)benzenecarbohydrazonoyl chloride収率 76.4%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

The title compound was prepared according to the procedure described in step-2 of Intermediate-1 using (1E)-1-(2-chloro-6-fluorobenzylidene)-2-(4-iodophenyl)hydrazine (1.2 g, 3.20 mmol), PCl5 (0.990 g, 4.8 mmol) and benzene (20 mL) to afford 1.0 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 7.00 (d, J=8.7 Hz, 2H), 7.41 (d, J=8.7 Hz, 1H), 7.48-7.60 (m, 4H), 10.22 (s, 1H).

後処理

  1. customThe title compound was prepared

出典と根拠

ORDレコード
ord-231b05ccd5da4598b900182a5680c4b5
出典データセット
uspto-grants-2015_08
特許番号
US09096545B2

関連ノート

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