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tert-Butanol → Tert-butyl [6-(3-{[3-(1-cyano-1-methylethyl)benzoyl]amino}phenoxy)imidazo[1,2-b]pyridazin-2-yl]carbamate

HRID 2391191
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HRID 2391191 반응식
[C:1]([C:3]([C:6]1[CH:7]=[C:8]([CH:31]=[CH:32][CH:33]=1)[C:9]([NH:11][C:12]1[CH:13]=[C:14]([CH:28]=[CH:29][CH:30]=1)[O:15][C:16]1[CH:17]=[CH:18][C:19]2[N:20]([CH:22]=[C:23](C(O)=O)[N:24]=2)[N:21]=1)=[O:10])([CH3:5])[CH3:4])#[N:2].C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:41])C=CC=CC=1.C([N:53]([CH2:56]C)CC)C.[C:58]([OH:62])([CH3:61])([CH3:60])[CH3:59]>>[C:1]([C:3]([C:6]1[CH:7]=[C:8]([CH:31]=[CH:32][CH:33]=1)[C:9]([NH:11][C:12]1[CH:13]=[C:14]([CH:28]=[CH:29][CH:30]=1)[O:15][C:16]1[CH:17]=[CH:18][C:19]2[N:20]([CH:22]=[C:23]([NH:53][C:56](=[O:41])[O:62][C:58]([CH3:61])([CH3:60])[CH3:59])[N:24]=2)[N:21]=1)=[O:10])([CH3:5])[CH3:4])#[N:2]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6386tert-ButanolHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 575054566-(3-{[3-(1-Cyano-1-methylethyl)benzoyl]amino}phenoxy)imidazo[1,2-b]pyridazine-2-carboxylic acid

생성물 1

HCID 57505457Tert-butyl [6-(3-{[3-(1-cyano-1-methylethyl)benzoyl]amino}phenoxy)imidazo[1,2-b]pyridazin-2-yl]carbamate수율 71%

실험 절차

Using 6-(3-{[3-(1-cyano-1-methylethyl)benzoyl]amino}phenoxy)imidazo[1,2-b]pyridazine-2-carboxylic acid (826 mg, 1.87 mmol), diphenylphosphoryl azide (771 mg, 2.81 mmol), triethylamine (381 mg, 3.74 mmol) and tert-butanol (30.0 mL), and in the same manner as in Example 64, the title compound (682 mg, 71%) was obtained as a white powder.

출처 및 근거

ORD 기록
ord-2eface3d95a04b8f9d25f2c6b78bff5b
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273741B2

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