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Trifluoroacetic acid → HCID 89962677, 화합물

HRID 337812
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HRID 337812 반응식
[C:1]([C:3]1[C:4]([O:31][C@H:32]2[CH2:36][CH2:35][CH2:34][C@@H:33]2[C:37]2[N:41]([CH3:42])[N:40]=[CH:39][CH:38]=2)=[CH:5][C:6]([F:30])=[C:7]([S:9]([N:12](CC2C=CC(OC)=CC=2OC)[C:13]2[CH:18]=[CH:17][N:16]=[CH:15][N:14]=2)(=[O:11])=[O:10])[CH:8]=1)#[N:2].C([SiH](CC)CC)C.FC(F)(F)C(O)=O>ClCCl>[C:1]([C:3]1[C:4]([O:31][C@H:32]2[CH2:36][CH2:35][CH2:34][C@@H:33]2[C:37]2[N:41]([CH3:42])[N:40]=[CH:39][CH:38]=2)=[CH:5][C:6]([F:30])=[C:7]([S:9]([NH:12][C:13]2[CH:18]=[CH:17][N:16]=[CH:15][N:14]=2)(=[O:10])=[O:11])[CH:8]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 12052TriethylsilaneHCID 89963038HCID 89963038, 화합물

생성물 1

HCID 89962677HCID 89962677, 화합물수율 89.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The reaction and aftertreatment were conducted in the same manner as in Example 1b by using the 5-cyano-N-(2,4-dimethoxybenzyl)-2-fluoro-4-{[(1S*,2R*)-2-(1-methyl-1H-pyrazol-5-yl)cyclopentyl]oxy}-N-(pyrimidin-4-yl)benzenesulfonamide (32.3 mg, 0.0545 mmol) prepared in Example 62d, triethylsilane (0.20 mL), trifluoroacetic acid (2.0 mL) and dichloromethane (2.0 mL), to yield the title compound (21.5 mg, 89%) as a colorless solid.

후처리

  1. customThe reaction and aftertreatment

출처 및 근거

ORD 기록
ord-75ceebbf63114e05872a83ab9a2e5808
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889741B2

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