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Trifluoroacetic acid → 5H-Benzo(6,7)cyclohepta(1,2-d)pyrimidin-2-amine, 4-((3R)-3-amino-1-pyrrolidinyl)-6,7-dihydro-

HRID 1014934
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HRID 1014934 반응식
C(OC([NH:8][C@@H:9]1[CH2:13][CH2:12][N:11]([C:14]2[C:15]3[CH2:25][CH2:24][CH2:23][C:22]4[CH:26]=[CH:27][CH:28]=[CH:29][C:21]=4[C:16]=3[N:17]=[C:18]([NH2:20])[N:19]=2)[CH2:10]1)=O)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:8][C@@H:9]1[CH2:13][CH2:12][N:11]([C:14]2[C:15]3[CH2:25][CH2:24][CH2:23][C:22]4[CH:26]=[CH:27][CH:28]=[CH:29][C:21]=4[C:16]=3[N:17]=[C:18]([NH2:20])[N:19]=2)[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 597768164-((3R)-3-(t-Butoxycarbonyl)Amino-pyrrolidin-1-yl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidin-2-ylamine

생성물 1

HCID 250687535H-Benzo(6,7)cyclohepta(1,2-d)pyrimidin-2-amine, 4-((3R)-3-amino-1-pyrrolidinyl)-6,7-dihydro-

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of the product from Example 4D (68 mg, 0.17 mmol) in CH2Cl2 (3 mL) was treated with trifluoroacetic acid (0.2 mL) and stirred for 16 hours. The mixture was diluted with CH2Cl2, washed H2O, dried, concentrated and chromatographed on silica gel eluting with eluting with NH4OH/MeOH/CH2Cl2 (0.8/8/92) to provide the title compound.

후처리

  1. washwashed H2O
  2. customdried
  3. concentrationconcentrated
  4. customchromatographed on silica gel eluting
  5. washwith eluting with NH4OH/MeOH/CH2Cl2 (0.8/8/92)

출처 및 근거

ORD 기록
ord-100f9f366c9d42f7af479d8a5f766996
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07985745B2

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