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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412473생성일: 2026년 10월 25일

Acetic Acid → (R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acid

https://huagongshe.com/reaction/412473

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-tert-ButylcyclohexylamineHCID 79396—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(R)-3-(4-Formylbenzoylamino)-2-hydroxypropionic acidHCID 86586064—
용매MethanolHCID 887—
용매Trimethyl orthoformateHCID 9005—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물(R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acidHCID 67485259—

반응 단계

The above resin bound (R)-3-(4-formylbenzoylamino)-2-hydroxypropionic acid was treated with a 0.5 M solution of 4-tert-butylcyclohexylamine (0.25 mmol) in a mixture of N-methyl-2-pyrrolidinone and trimethylorthoformate (1:1, 0.5 mL) and glacial acetic acid (50 μL) for 1 hour at 25° C. Sodium cyanoborohydride (250 μmol, 16 mg) dissolved in a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 0.25 mL) was added and the mixture was vortexed at 25° C. for 4 hours followed by filtration and washing with a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 2×1 mL) 3×1 mL N-methyl-2-pyrrolidinone (3×1 mL) and a mixture of 1,2-dichloropropane and diisopropylethylamine (7:1, 2×0.75 mL).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562807B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-fa4a1c5ab51e473fb5cb99043408e8c8
출처 메모uspto-grants-2003_05