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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 178433201, 화합물

HRID 378993
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반응식

HRID 378993 반응식
[NH:1]([C:5]1[S:6][C:7]([C:11]([NH:13][C:14]2[CH:15]=[C:16]([CH:26]=[CH:27][CH:28]=2)[O:17][CH2:18][C:19]([O:21]C(C)(C)C)=[O:20])=[O:12])=[C:8]([CH3:10])[N:9]=1)[C:2]([NH2:4])=[NH:3].FC(F)(F)C(O)=O>C(Cl)Cl>[NH:1]([C:5]1[S:6][C:7]([C:11]([NH:13][C:14]2[CH:15]=[C:16]([CH:26]=[CH:27][CH:28]=2)[O:17][CH2:18][C:19]([OH:21])=[O:20])=[O:12])=[C:8]([CH3:10])[N:9]=1)[C:2]([NH2:4])=[NH:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 178433202HCID 178433202, 화합물

생성물 1

HCID 178433201HCID 178433201, 화합물수율 82.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

142 mg of tert-butyl {3-[(2-guanidino-4-methyl-thiazole-5-carbonyl)-amino]-phenoxy}-acetate is stirred in 1.1 ml of methylene chloride and 1.1 ml of trifluoroacetic acid (TFA) for 2 hrs. at RT. The reaction mixture is evaporated in a vacuum, the residue is taken up in water and the solution is evaporated to dryness. The solid is suspended in water, adjusted to pH 8 with 1N ammonia while stirring, filtered off under suction, washed with water and dried. There are obtained 101 mg of [3-[(2-guanidino-4-methyl-thiazole-5-carbonyl)-amino]-phenoxy]-acetic acid, m.p. 284° C., MS: 350 (M+H)+.

후처리

  1. customat RT
  2. customThe reaction mixture is evaporated in a vacuum
  3. customthe solution is evaporated to dryness
  4. filtrationfiltered off under suction
  5. washwashed with water
  6. customdried

출처 및 근거

ORD 기록
ord-51ead022fbaf44de891b4b0d6a9829bd
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06297266B1

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