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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 68556345, 화합물

HRID 2370280
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반응식

HRID 2370280 반응식
C(OC(=O)[NH:7][C:8]1([CH2:22][CH2:23][CH2:24][O:25][CH3:26])[CH2:13][CH2:12][CH:11]([O:14][Si](C(C)(C)C)(C)C)[CH2:10][CH2:9]1)(C)(C)C.FC(F)(F)C(O)=O.Cl>ClCCl>[NH2:7][C:8]1([CH2:22][CH2:23][CH2:24][O:25][CH3:26])[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 68548643HCID 68548643, 화합물

생성물 1

HCID 68556345HCID 68556345, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

200 mg of the crude [4-(tert-butyl-dimethyl-silanyloxy)-1-(3-methoxy-propyl)-cyclohexyl]-carbamic acid tert-butyl ester (33, step a) were dissolved in 10 mL of dichloromethane and treated with 370 μL of trifluoroacetic acid. After stirring at room temperature until complete conversion was achieved, 2M aqueous hydrochloric acid was added, the mixture stirred for further 60 min and the aqueous phase evaporated. The crude aminoalcohol was lyophilized from water and used crude as hydrochloride in the next reaction. Rt=0.18 min, 0.37 min (Method C). Detected mass: 188.3 (M+H+).

후처리

  1. stirringthe mixture stirred for further 60 min
  2. customthe aqueous phase evaporated
  3. customin the next reaction
  4. customRt=0.18 min, 0.37 min (Method C)

출처 및 근거

ORD 기록
ord-2309a68d2aad4703825902f2896b62db
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08710077B2

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