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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 847306생성일: 2026년 10월 25일

Triethylamine → HCID 178501427, 화합물

https://huagongshe.com/reaction/847306

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물(R)-alpha-(pivaloylmethyl)hydrocinnamic acidHCID 18611819—
반응물HCID 178419105HCID 178419105—
용매DimethylformamideHCID 6228—
생성물HCID 178501427HCID 17850142781.9%

반응 단계

A suspension of 3.0 g (12 mmol) of (R)-α-(pivaloylmethyl)hydrocinnamic acid (see EPA 0,184,550) and 2.66 g (11 mmol) of L-histidine methyl ester dihydrochloride in 340 ml of dimethylformamide is treated at room temperature under a nitrogen atmosphere with 3.45 g (34 mmol) of triethylamine and 4.58 g (12 mmol) of HBTU. The reaction mixture is stirred at room temperature for 5 hours and subsequently evaporated in a high vacuum. The residue is dissolved in 500 ml of ethyl acetate and washed in succession with 100 ml of water, three times with 100 ml of saturated sodium bicarbonate solution each time and 100 ml of saturated sodium chloride solution. The organic phase is dried over sodium sulphate, evaporated under reduced pressure and the yellowish crude product obtained is chromatographed on silica gel with a 95:5 mixture of methylene chloride and methanol which contains 0.1% ammonia. In this manner there are obtained 3.6 g N-[(R)-α-(3,3-dimethyl-2-oxobutyl)hydrocinnamoyl]-L-histidine methyl ester as a colourless foam, MS: 399 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05140011
출처 데이터셋uspto-grants-1992_08
ORD IDord-0910ead46ce9497f952ecfe413a09592
출처 메모uspto-grants-1992_08