Water → HCID 178496106, 화합물

HRID 2214970

반응식

HRID 2214970 반응식
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH2:18][O:19][CH3:20])=[CH:12][CH:11]=2)[C:5]([C:21]#[N:22])=[C:4]([SH:23])[N:3]=1.[C:24](=O)(O)[O-].[Na+].ClC[C:31]1[N:32]=[C:33]([C:36]2[CH:40]=[CH:39][S:38][CH:37]=2)[S:34][CH:35]=1.O>CN(C=O)C>[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([C:10]2[CH:11]=[CH:12][C:13]([O:16][CH2:17][CH2:18][O:19][CH3:20])=[CH:14][CH:15]=2)[C:5]([C:21]#[N:22])=[C:4]([SH:23]([C:31]2[N:32]=[C:33]([C:36]3[CH:40]=[CH:39][S:38][CH:37]=3)[S:34][CH:35]=2)[CH3:24])[N:3]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 516892Sodium BicarbonateHCID 6021074-(Chloromethyl)-2-(thiophen-3-yl)-1,3-thiazoleHCID 178496105HCID 178496105, 화합물

생성물 1

HCID 178496106HCID 178496106, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

100 mg (0.31 mmol) of 2-amino-4-[4-(2-methoxyethoxy)phenyl]-6-sulphanyl-pyridine-3,5-dicarbonitrile are dissolved in 1 ml of DMF. 103 mg (1.23 mmol) of sodium bicarbonate and 96.4 mg (0.46 mmol) of 4-chloromethyl-2-(thiophen-3-yl)-1,3-thiazole are then added. The suspension is shaken at RT overnight, and water is added. The precipitate is filtered off with suction, washed with ethanol and diethyl ether and dried at 40° C. under reduced pressure. This gives 141 mg (82% of theory) of product.

후처리

  1. filtrationThe precipitate is filtered off with suction
  2. washwashed with ethanol and diethyl ether
  3. customdried at 40° C. under reduced pressure

출처 및 근거

ORD 기록
ord-569f1ae26e884bb18752602897058329
출처 데이터셋
uspto-grants-2006_09
특허 번호
US07109218B2

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