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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854653생성일: 2026년 10월 26일

Ammonium Chloride → tert-butyl (S)-3-methyl-2-{[cis-3-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)cyclohexylmethyl]amino}butyrate

https://huagongshe.com/reaction/854653

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물tert-Butyl L-valinateHCID 114626—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물cis-3-(5-Methyl-2-p-tolyloxazol-4-ylmethoxy)cyclohexanecarbaldehydeHCID 86597945—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물tert-butyl (S)-3-methyl-2-{[cis-3-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)cyclohexylmethyl]amino}butyrateHCID 8659794499%

반응 조건

온도0 °C

반응 단계

511 mg of cis-3-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)cyclohexanecarbaldehyde, 0.9 ml of HOAc and 310 mg of tert-butyl (S)-valinate are dissolved in 5 ml of abs. dichloromethane. 500 mg of molecular sieve 4 Å are then added, and the suspension is cooled to 0° C. 414 mg of sodium triacetoxyborohydride are added a little at a time. This suspension is stirred at 0° C. for 2 h, 3 ml of saturated NH4Cl solution are then added and the suspension is stirred for a further 10 min. In each case 10 ml of water and dichloromethane are added, the phases are separated, the aqueous phase is extracted with dichloromethane and the combined organic phases are dried over MgSO4 and concentrated, which gives 760 mg of tert-butyl (S)-3-methyl-2-{[cis-3-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)cyclohexylmethyl]-amino}butyrate. C28H42N2O4 (470.66); MS (ESI): 471.50 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259177B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-09f64f4ba2fe44ccb7115b1bf25fc90f
출처 메모uspto-grants-2007_08