홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrochloric Acid → 6-(Carbamoyl-fluoro-methyl)benzo[b]thiophene-2-carboxylic acid

HRID 1172898
노트
인쇄 미리보기

반응식

HRID 1172898 반응식
C([O:3][C:4]([C:6]1[S:10][C:9]2[CH:11]=[C:12]([CH:15]([C:17](=[O:19])[NH2:18])[F:16])[CH:13]=[CH:14][C:8]=2[CH:7]=1)=[O:5])C.[Li+].[OH-].Cl>CO.C1COCC1>[C:17]([CH:15]([F:16])[C:12]1[CH:13]=[CH:14][C:8]2[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[S:10][C:9]=2[CH:11]=1)(=[O:19])[NH2:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 595564086-(Carbamoyl-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl ester

생성물 1

HCID 595564146-(Carbamoyl-fluoro-methyl)benzo[b]thiophene-2-carboxylic acid

시약·촉매·용매 1

HCID 21899815MeOH tetrahydrofuran용매

실험 절차

To a solution of 6-(carbamoyl-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl ester (295 mg, 1.05 mmol) in MeOH/THF (1.5/6 mL) was added 1M LiOH (1.16 mL). The resultant solution was stirred overnight and 1N HCl was added dropwise to acidify (˜2 mL). The solvent was removed in vacuo and the solid was used without further purification. cal'd 254 (MH+), exp 254 (MH+).

후처리

  1. customThe solvent was removed in vacuo
  2. customthe solid was used without further purification

출처 및 근거

ORD 기록
ord-39a5a77b3c6741fb9f3060019c48440c
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07834034B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트