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

Triethylamine → (3aR*,10aS*)-4-(Phthalimidoacetyl)-9-(4-propionamidobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

HRID 361577
노트
인쇄 미리보기

반응식

HRID 361577 반응식
[NH2:1][C:2]1[CH:37]=[CH:36][C:5]([CH2:6][N:7]2[C:13](=[O:14])[C@H:12]3[CH2:15][CH2:16][CH2:17][C@H:11]3[N:10]([C:18](=[O:31])[CH2:19][N:20]3[C:24](=[O:25])[C:23]4=[CH:26][CH:27]=[CH:28][CH:29]=[C:22]4[C:21]3=[O:30])[C:9]3[CH:32]=[CH:33][CH:34]=[CH:35][C:8]2=3)=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:45](Cl)(=[O:48])[CH2:46][CH3:47]>ClCCl.O>[C:21]1(=[O:30])[N:20]([CH2:19][C:18]([N:10]2[C@@H:11]3[CH2:17][CH2:16][CH2:15][C@@H:12]3[C:13](=[O:14])[N:7]([CH2:6][C:5]3[CH:4]=[CH:3][C:2]([NH:1][C:45](=[O:48])[CH2:46][CH3:47])=[CH:37][CH:36]=3)[C:8]3[CH:35]=[CH:34][CH:33]=[CH:32][C:9]2=3)=[O:31])[C:24](=[O:25])[C:23]2=[CH:26][CH:27]=[CH:28][CH:29]=[C:22]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 62324Propionyl chlorideHCID 54523300(3aR*,10aS*)-9-(4-aminobenzyl)-4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][l,4]diazepin-10(1H)-one

생성물 1

HCID 67767989(3aR*,10aS*)-4-(Phthalimidoacetyl)-9-(4-propionamidobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one수율 79.3%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6344Dichloromethane용매

실험 절차

To a suspension of (3aR*,10aS*)-9-(4-aminobenzyl)-4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][l,4]diazepin-10(1H)-one (148 mg, 0.3 mmol) and triethylamine (50 μL, 0.36 mmol) in dichloromethane (3 mL) was added propionyl chloride (28 μL, 0.33 mmol) and the mixture was stirred at room temperature for 10 minutes. This reaction mixture was diluted with water and stirred. The aqueous layer was separated and the organic layer was dried over NaSO4 and concentrated under reduced pressure. The residue was crystallized from dichloromethane-ethanol-diethyl ether to provide 131 mg (yield 79%) of the title compound. m.p. 286.0°-286.5° C.

후처리

  1. stirringstirred
  2. customThe aqueous layer was separated
  3. dry with materialthe organic layer was dried over NaSO4
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was crystallized from dichloromethane-ethanol-diethyl ether

출처 및 근거

ORD 기록
ord-265c5f384d0d4cbdba604d00b76c034f
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866567

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트