(3S)-pyrrolidin-3-ol → HCID 46701789, compound

HRID 2090370Notes

Reaction equation

HRID 2090370 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([N:8]2[CH:17]([CH3:18])[CH2:16][C:15]3[C:10](=[CH:11][C:12]([C:19]4[CH:24]=[CH:23][N:22]=[C:21]([C:25]([OH:27])=O)[CH:20]=4)=[CH:13][CH:14]=3)[CH2:9]2)[CH:5]=[C:4]([N:28]2[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]2)[N:3]=1.[OH:35][C@H:36]1[CH2:40][CH2:39][NH:38][CH2:37]1>>[NH2:1][C:2]1[N:7]=[C:6]([N:8]2[CH:17]([CH3:18])[CH2:16][C:15]3[C:10](=[CH:11][C:12]([C:19]4[CH:24]=[CH:23][N:22]=[C:21]([C:25]([N:38]5[CH2:39][CH2:40][C@H:36]([OH:35])[CH2:37]5)=[O:27])[CH:20]=4)=[CH:13][CH:14]=3)[CH2:9]2)[CH:5]=[C:4]([N:28]2[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]2)[N:3]=1

Participants

3

Reactant 2

HCID 2733874(3S)-pyrrolidin-3-olHCID 594023354-{2-[2-Amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3-methyl-1,2,3,4-tetrahydroisoquinolin-7-yl}pyridine-2-carboxylic acid

Product 1

HCID 46701789HCID 46701789, compound

Procedure

This compound was prepared by using procedures analogous to those described for the synthesis of Example 61A starting from 4-{2-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3-methyl-1,2,3,4-tetrahydroisoquinolin-7-yl}pyridine-2-carboxylic acid (Example 61A, Step 2) and (S)-(−)-3-Hydroxypyrrolidine (Fluka, Cat. No. 56437). LCMS (M+H)+: m/z=529.3.

Workup

  1. customThis compound was prepared
  2. customthose described for the synthesis of Example 61A

Sources & evidence

ORD record
ord-c180a0c7fa5d47a1bbc1beb668dd7d0b
Source dataset
uspto-grants-2013_05
Patent number
US08436008B2

Reaction notes

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