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

Ammonium Chloride → rac-ethyl 2-((4S,6S,7R)-4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate

HRID 1748810
노트
인쇄 미리보기

반응식

HRID 1748810 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[S:14][CH:13]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:12]([CH3:21])=[N:11][C:10]3[N:22]([CH3:26])[N:23]=[C:24]([CH3:25])[C:9]2=3)=[C:4]([CH3:27])[CH:3]=1.[BH4-].[Na+].[NH4+].[Cl-]>CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[S:14][C@@H:13]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C@@H:12]([CH3:21])[NH:11][C:10]3[N:22]([CH3:26])[N:23]=[C:24]([CH3:25])[C:9]2=3)=[C:4]([CH3:27])[CH:3]=1.[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]2[S:14][C@@H:13]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C@@H:12]([CH3:21])[NH:11][C:10]3[N:22]([CH3:26])[N:23]=[C:24]([CH3:25])[C:9]2=3)=[C:4]([CH3:27])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 86724138ethyl 2-(4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6-dihydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate

생성물 2

HCID 136634675rac-ethyl 2-((4R,6S,7R)-4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate수율 19%
HCID 136634681
rac-ethyl 2-((4S,6S,7R)-4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate
수율 49%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of ethyl 2-(4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6-dihydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate (0.85 g, 1.97 mmol) in MeOH (3.94 mL) was cooled to about 0° C. To the reaction mixture was added sodium tetrahydroborate (0.298 g, 7.88 mmol) portionwise. The reaction mixture was allowed to slowly warm to ambient temperature and stirred for about 16 h. The reaction mixture was cooled to about 0° C. and then saturated aqueous NH4Cl (10 mL) was added. The mixture was partially concentrated under reduced pressure and EtOAc (20 mL) was added. The layers were separated and the aqueous layer was back extracted with EtOAc (10 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography (SiO2, EtOAc/DCM 100:0 to 0:50) to afford rac-ethyl 2-((4R,6S,7R)-4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate (0.15 g, 0.37 mmol, 19%) LC-MS (Table 1, Method g) Rt=2.58, m/z 408 (M+H)+and rac-ethyl 2-((4S,6S,7R)-4-(4-chloro-2-methylphenyl)-1,3,7-trimethyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-e][1,4]thiazepin-6-yl)acetate (0.39 g, 0.97 mmol, 49%) LC-MS (Table 1, Method g) Rt=2.48, m/z 408 (M+H)+.

후처리

  1. temperatureThe reaction mixture was cooled to about 0° C.
  2. concentrationThe mixture was partially concentrated under reduced pressure and EtOAc (20 mL)
  3. additionwas added
  4. customThe layers were separated
  5. extractionthe aqueous layer was back extracted with EtOAc (10 mL)
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe crude material was purified by column chromatography (SiO2, EtOAc/DCM 100:0 to 0:50)

출처 및 근거

ORD 기록
ord-a4dfb2de52934e6eb97cc443576b5954
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150592B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트