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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 4-[4-(Cyclopropylmethyl-amino)-pyrimidin-2-yl]-benzylamine

HRID 1191103
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인쇄 미리보기

반응식

HRID 1191103 반응식
[CH:1]1([CH2:4][NH:5][C:6]2[CH:11]=[CH:10][N:9]=[C:8]([C:12]3[CH:26]=[CH:25][C:15]([CH2:16][NH:17]C(OC(C)(C)C)=O)=[CH:14][CH:13]=3)[N:7]=2)[CH2:3][CH2:2]1.FC(F)(F)C(O)=O>C(Cl)Cl>[CH:1]1([CH2:4][NH:5][C:6]2[CH:11]=[CH:10][N:9]=[C:8]([C:12]3[CH:13]=[CH:14][C:15]([CH2:16][NH2:17])=[CH:25][CH:26]=3)[N:7]=2)[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 58495645HCID 58495645, 화합물

생성물 1

HCID 584956304-[4-(Cyclopropylmethyl-amino)-pyrimidin-2-yl]-benzylamine수율 96.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Dissolve 4-[4-(cyclopropylmethyl-amino)-pyrimidin-2-yl]-N-(tert-butoxycarbonyl)-benzylamine (100 mg, 0.28 mmol) in DCM (3 mL) containing trifluoroacetic acid (2 mL). Stir under nitrogen for 3 h. Concentrate in vacuo and purify the crude mixture by SCX chromatography (5 g) to obtain the title compound (68.5 mg, 90%) suitable for use without additional purification. MS (ES+) m/z: 255 (M+H)+.

후처리

  1. concentrationConcentrate in vacuo
  2. custompurify the crude mixture by SCX chromatography (5 g)

출처 및 근거

ORD 기록
ord-4b0b3de746a448b5a31b10ea8207b7bd
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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