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4-Toluenesulfonyl chloride → 5-(N'-cyano-N"-methylguanidino)pentyl p-toluenesulphonate

HRID 261835
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HRID 261835 반응식
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[C:12]([NH:14][C:15]([NH:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][OH:24])=[N:16][CH3:17])#[N:13]>N1C=CC=CC=1>[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7]([O:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][NH:18][C:15]([NH:16][CH3:17])=[N:14][C:12]#[N:13])(=[O:9])=[O:8])=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 73974-Toluenesulfonyl chlorideHCID 54552768N-cyano-N'-(5-hydroxypentyl)-N"-methylguanidine

생성물 1

HCID 1784850465-(N'-cyano-N"-methylguanidino)pentyl p-toluenesulphonate수율 42.9%

시약·촉매·용매 1

HCID 1049Pyridine용매2회

실험 절차

A solution of p-toluenesulphonyl chloride (9.11 g) in pyridine (40 ml) was added in portions to a stirred solution of N-cyano-N'-(5-hydroxypentyl)-N"-methylguanidine (8.0 g) in pyridine (40 ml) at -10°. The mixture was stirred at 2° for 40 hours and was poured into ice-water. The aqueous mixture was extracted with chloroform, and the extracts were washed with dilute hydrochloric acid and evaporated to give 5-(N'-cyano-N"-methylguanidino)pentyl p-toluenesulphonate (6.3 g) as an orange oil.

후처리

  1. extractionThe aqueous mixture was extracted with chloroform
  2. washthe extracts were washed with dilute hydrochloric acid
  3. customevaporated

출처 및 근거

ORD 기록
ord-0a16af7e791f43249b4401bbd19d1a24
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04152453

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