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HCID 86699023, 화합물 → HCID 178462332, 화합물

HRID 1424171
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반응식

HRID 1424171 반응식
C(OC([N:8]1[C@@H:12]([C:13](O)=O)[C@@H:11]([CH3:16])[O:10]C1(C)C)=O)(C)(C)C.[NH2:19][C:20]1[CH:21]=[C:22]([C:27]2[CH:32]=[CH:31][C:30]([C:33]#[N:34])=[CH:29][CH:28]=2)[CH:23]=[CH:24][C:25]=1[NH2:26]>>[NH2:8][C@@H:12]([C:13]1[NH:26][C:25]2[CH:24]=[CH:23][C:22]([C:27]3[CH:32]=[CH:31][C:30]([C:33]#[N:34])=[CH:29][CH:28]=3)=[CH:21][C:20]=2[N:19]=1)[C@H:11]([OH:10])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 86699023HCID 86699023, 화합물HCID 86699075HCID 86699075, 화합물

생성물 1

HCID 178462332HCID 178462332, 화합물

실험 절차

The title compound was prepared according to Method 4 using (4R,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidine-4-carboxylic acid (Preparation 59A) and 3′,4′-diaminobiphenyl-4-carbonitrile (Preparation 82). The reaction mixture was concentrated in vacuo and purified by SCX-2 cartridge (16 mg, 72%).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. custompurified by SCX-2 cartridge (16 mg, 72%)

출처 및 근거

ORD 기록
ord-940e6bbb6e86463baa1a7407ecb14986
출처 데이터셋
uspto-grants-2015_01
DOI
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
10.6084/m9.figshare.5104873.v1
특허 번호
US08927587B2

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