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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47729생성일: 2026년 10월 23일

Hydrochloric Acid → (+)-(4R)-4-(4-aminobutyl)-4,5-dihydro-1,3-thiazol-2-ylamine dihydrochloride

https://huagongshe.com/ko/reaction/47729

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물benzyl (5R)-5-{[(tert-butylamino)carbothioyl]amino}-6-hydroxyhexylcarbamateHCID 86584427—
용매EthanolHCID 702—
생성물(+)-(4R)-4-(4-aminobutyl)-4,5-dihydro-1,3-thiazol-2-ylamine dihydrochlorideHCID 69885654—

반응 단계

The process is performed as in Example 1, starting with 5.9 g of benzyl (5R)-5-{[(tert-butylamino)carbothioyl]amino}-6-hydroxyhexylcarbamate in 40 cm3 of aqueous 6N hydrochloric acid at a temperature in the region of 100° C. for 3 hours. After concentration of the reaction medium under reduced pressure (5 kPa) at a temperature in the region of 50° C., the residue obtained is taken up in ethanol and then concentrated again under the above conditions. The paste obtained is crystallized by trituration from an ethanol/methanol mixture (8/2 by volume). The crystals are filtered off, washed with acetonitrile and air-dried. 1.3 g of (+)-(4R)-4-(4-aminobutyl)-4,5-dihydro-1,3-thiazol-2-ylamine dihydrochloride are obtained in the form of a white solid melting at 188° C. (αD20=+16.2±0.7 at a concentration of 0.5% in methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699895B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-60932a1560cb45749a343713bab42d5f
출처 메모uspto-grants-2004_03