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Ammonia → (1S,4S)-4-[3-((S)-2-Methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-ylamine

HRID 631011
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HRID 631011 반응식
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C@@H:5]([OH:12])[CH2:4][CH2:3]1.[Na].F[C:15]1[CH:16]=[CH:17][C:18]2[N:19]([C:21]([N:24]3[CH2:29][CH2:28][CH2:27][CH2:26][C@@H:25]3[CH3:30])=[N:22][N:23]=2)[CH:20]=1.N>CN(C=O)C.CO.C(Cl)Cl>[CH3:30][C@H:25]1[CH2:26][CH2:27][CH2:28][CH2:29][N:24]1[C:21]1[N:19]2[CH:20]=[C:15]([O:12][C@@H:5]3[C:6]4[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=4)[C@@H:2]([NH2:1])[CH2:3][CH2:4]3)[CH:16]=[CH:17][C:18]2=[N:23][N:22]=1
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참가 물질

8

반응물 4

HCID 222AmmoniaHCID 5360545SodiumHCID 86686682(1S,4S)-4-amino-1,2,3,4-tetrahydronaphthalen-1-olHCID 866871056-Fluoro-3-((S)-2-methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridine

생성물 1

HCID 86687322(1S,4S)-4-[3-((S)-2-Methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-ylamine수율 47.5%

시약·촉매·용매

3
HCID 887Methanol용매HCID 6228Dimethylformamide용매2회HCID 6344Dichloromethane용매

실험 절차

To a solution of Intermediate B (232 mg, 1.6 mmol) in dry DMF (10 mL) under N2 was added sodium (60% dispersion in oil, 320 mg, 8.0 mmol) and the resulting opaque brown solution was stirred at RT for 45 min (CARE: gas evolution). A solution of Intermediate 81c (342 mg, 1.46 mmol) in dry DMF (7 mL) was added and the dark brown solution stirred at 60° C. under N2 for 90 min. The cooled solution was concentrated in vacuo, redissolved in MeOH (3 mL) and then applied to an SCX-2 cartridge (20 g), washing with MeOH (50 mL). The product was eluted with 2M NH3 in MeOH (50 mL); concentration in vacuo gave a dark brown solid. FCC, using 0-10% [2M NH3 in MeOH] in DCM, gave the title compound as a pale brown foam (262 mg, 45%). LCMS (Method 3): Rt 2.30 min, m/z 378 [MH+].

후처리

  1. stirringthe dark brown solution stirred at 60° C. under N2 for 90 min
  2. concentrationThe cooled solution was concentrated in vacuo
  3. dissolutionredissolved in MeOH (3 mL)
  4. washwashing with MeOH (50 mL)
  5. washThe product was eluted with 2M NH3 in MeOH (50 mL)
  6. concentrationconcentration in vacuo
  7. customgave a dark brown solid

출처 및 근거

ORD 기록
ord-b9fa1b01c3664b48a3822bd9b64578fb
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315503B2

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