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

Triethylamine → 6-bromo-N-(cyclohexylmethyl)benzo[d]thiazol-2-amine

HRID 2077605
노트
인쇄 미리보기

반응식

HRID 2077605 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7](Cl)[S:8][C:4]=2[CH:3]=1.[CH:12]1([CH2:18][NH2:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1.C(N(CC)CC)C>CN(C=O)C>[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH:19][CH2:18][CH:12]3[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]3)[S:8][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 76688CyclohexanemethylamineHCID 20498716-Bromo-2-chlorobenzothiazole

생성물 1

HCID 772315086-bromo-N-(cyclohexylmethyl)benzo[d]thiazol-2-amine수율 61%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A microwave reaction vial was charged with 6-bromo-2-chlorobenzo[d]thiazole (300 mg, 1.21 mmol), cyclohexylmethanamine (143 mg, 1.27 mmol), triethylamine (183 mg, 1.81 mmol) and 2.4 mL DMF. The vial was sealed, and the mixture was irradiated in the microwave for 20 min at 150° C. The reaction mixture was concentrated twice from toluene and purified by silica gel chromatography (0-50% 90/10 CH2Cl2/MeOH in CH2Cl2), which provided 6-bromo-N-(cyclohexylmethyl)benzo[d]thiazol-2-amine (240 mg, 61%) as a white solid. MS (ESI pos. ion) m/z calc'd for C14H17BrN2S: 325.3/327.3. found 325.0/327.0.

후처리

  1. customA microwave reaction
  2. customThe vial was sealed
  3. customthe mixture was irradiated in the microwave for 20 min at 150° C
  4. concentrationThe reaction mixture was concentrated twice from toluene
  5. custompurified by silica gel chromatography (0-50% 90/10 CH2Cl2/MeOH in CH2Cl2), which

출처 및 근거

ORD 기록
ord-76541761dcba4111b78a8ae641fd736c
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928140B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트