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HCID 67397745, 화합물 → HCID 67399150, 화합물

HRID 914390
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HRID 914390 반응식
[CH2:1]([NH:8][C:9](=O)[CH2:10][C:11]1[N:12]=[C:13]([S:16][C:17]([CH3:22])([CH3:21])[C:18]([OH:20])=[O:19])[S:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]>O1CCCC1>[CH2:1]([NH:8][CH2:9][CH2:10][C:11]1[N:12]=[C:13]([S:16][C:17]([CH3:21])([CH3:22])[C:18]([OH:20])=[O:19])[S:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 67397745HCID 67397745, 화합물

생성물 1

HCID 67399150HCID 67399150, 화합물수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a suspension of 2-({4-[2-(heptylamino)-2-oxoethyl]-1,3-thiazol-2-yl}thio)-2-methylpropionic acid resin (5.2 g) synthesized in Example 461-5 in tetrahydrofuran (20 mL) was added 1 mol/L borane-tetrahydrofuran complex (18 ml), and the mixture was stirred at room temperature for 30 min, and at 50° C. for 16.5 hr. The resin was collected by filtration from the mixture, washed three times each with tetrahydrofuran and methanol, and vacuum dried to give the title pale-yellow resin (4.0 g).

후처리

  1. additionwas added 1 mol/L borane-tetrahydrofuran complex (18 ml)
  2. waitat 50° C. for 16.5 hr
filtration
The resin was collected by filtration from the mixture
  • washwashed three times each with tetrahydrofuran and methanol, and vacuum
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-0f262ee443b543f1823a35dc4c7106b9
    출처 데이터셋
    uspto-grants-2011_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08026370B2

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