돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1835614생성일: 2026년 10월 27일

Propylamine → 4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine

https://huagongshe.com/reaction/1835614

반응식

참여 물질

역할이름HCID투입량
반응물PropylamineHCID 7852—
반응물Propylamine hydrochlorideHCID 11165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-Amino-4,5,6,7-tetrahydro-1,3-benzothiazol-4-oneHCID 21941906—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamineHCID 4885—

반응 단계

3.0 g of propylamine hydrochloride was dissolved in 60 mL of methanol and 2.2 g of 2-amino-oxo-4,5,6,7-tetrahydrobenzothiazole was added. 1.1 mL of propylamine was poured into the mixture to set pH within the range 6.5-7.0. Then 0.7 g of sodium cyanoborohydride was added and the reaction mixture was stirred for 70 hours under nitrogen atmosphere and at ambient temperature. The reaction mixture was diluted with 50 mL of water and 10 mL of conc. hydrochloric acid. Solvents were removed by evaporation, the yellow residue was stirred with ethanol and the solid was removed by filtration. The filtrate was made alkaline with potassium hydroxide solution and the precipitate was again removed by filtration. Filtrate was several times evaporated with ethanol to remove propylamine. The residue was dissolved in hot ethanol and resulting crystals were collected and dried. Reaction product was characterised by NMR spectra.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06770761B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-58a982f04be04b1097e3883a50b68d01
출처 메모uspto-grants-2004_08