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Potassium Bromide → HCID 69518987, 화합물

HRID 1831338
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HRID 1831338 반응식
Cl[C:2]([O:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][N:13]=2)=[CH:7][CH:6]=1)=[O:3].[Cl:22][C:23]1[S:27][C:26]([CH2:28][N:29]2[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]2)=[CH:25][CH:24]=1.[K+].[Br-]>CCO>[F:19][C:18]([F:21])([F:20])[C:15]1[CH:16]=[CH:17][C:12]([O:11][C:8]2[CH:9]=[CH:10][C:5]([O:4][C:2]([N:32]3[CH2:33][CH2:34][N:29]([CH2:28][C:26]4[S:27][C:23]([Cl:22])=[CH:24][CH:25]=4)[CH2:30][CH2:31]3)=[O:3])=[CH:6][CH:7]=2)=[N:13][CH:14]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 253877Potassium BromideHCID 24550121-[(5-Chloro-2-thienyl)methyl]piperazineHCID 220477624-(5-Trifluoromethylpyridin-2-yloxy)-phenyl chloroformate

생성물 1

HCID 69518987HCID 69518987, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The hydrochloride of the title compound was prepared from 4-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl chloroformate and 1-(5-chloro-thiophen-2-ylmethyl)-piperazine, yield 48%. White crystals, m.p. 225–226° C. (from EtOH); 1H NMR (DMSO-d6): δ 12.00 (br, 1H), 8.60–8.55 (1H), 8.27–8.21 (dd-like, 1H), 7.33–7.20 (m, 6H), 7.20–7.15 (d, 1H), 4.55 (br s, 2H), 4.40–4.00 (br, 2H), 3.74–3.27 (br, 4H+H2O); 3.27–2.97 (br, 2H); IR (KBr): ν 1723 (C═O) cm−1.

출처 및 근거

ORD 기록
ord-a4af7849047240b18630a79f5d5e4fc2
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067517B2

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