Phenyl Isothiocyanate → N-4-chlorobenzyl-N-cyclopentyl-N'-phenylthiourea

HRID 1704752

反応式

HRID 1704752 の反応式
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][NH:7][CH:8]2[CH2:12][CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[C:15]1([N:21]=[C:22]=[S:23])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]([CH:8]2[CH2:12][CH2:11][CH2:10][CH2:9]2)[C:22]([NH:21][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[S:23])=[CH:13][CH:14]=1

参加物

3

反応物 2

HCID 7673Phenyl IsothiocyanateHCID 8340834-chloro-N-cyclopentylbenzylamine

生成物 1

HCID 13018271N-4-chlorobenzyl-N-cyclopentyl-N'-phenylthiourea収率 92.8%

実験手順

Analogously to Example 1, 21 grams (0.1 mole) of N-4-chlorobenzyl-N-cyclopentylamine were reacted with 13.5 grams (0.1 mole) of phenylisothiocyanate. 32 grams of N-4-chlorobenzyl-N-cyclopentyl-N'-phenylthiourea were obtained. Yield: 92%, Melting point: 129°-132° C.

出典と根拠

ORDレコード
ord-c45d45730c5d4b50b13b1fe0493dcdd3
出典データセット
uspto-grants-1978_11
特許番号
US04127673

関連ノート

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